Products – Sansure Biotech

Brief

SLAN-96H, the avant-garde leader in real-time fluorescent quantitative PCR analysis, is designed for on-the-go testing, simplifying even the most complex procedures into effortless tasks. With a sleek and portable design that fits easily into a backpack, it empowers molecular detection to be conducted with unmatched ease and precision. This technology elevates the testing experience to a new level of convenience and efficiency. Revolutionary temperature control technology 1. Amplification takes only 30 minutes, approximately half the time of conventional PCR instruments. 2. It enables the rapid and accurate detection of gene expression variations as minimal as 2-fold. Smart Portable Design 1. Weighing under 10 kg, the instrument is one-third the weight of conventional thermal cyclers and can be carried in a backpack for molecular detection. 2. The instrument is operational without calibration after relocation. Interoperable Open Platform Compatible with various reagents, the device allows for customized experiments.

Eight-color fluorescence detection system Detects up to 8 targets per well, enhancing efficiency.

Robust Software System The software offers various analysis modes, including qualitative/absolute quantification, melt curve analysis, endpoint genotyping, HRM analysis, isothermal amplification, etc.

Specifications

Performance

Sample Capacity	96 wells (1×96-well×0.2 mL)
Consumables	0.2mL PCR tubes, 8-tube strip
Light Source	High power LED (Maintenance-free)
Detector	High sensitivity photoelectric sensor
Dynamic Range	10⁰ - 10¹⁰
Sensitivity	1 copy
Quantitative Repeatability	CV≤2.00%
Correlation	\|r\|≥0.9990
Concentration Differentiation	2-fold
Sample Volume	15μL - 100μL
Probe/Dye	Channel 1: FAM, SYBR-Green Channel 2:VIC, HEX, JOE, TET Channel 3: ROX, Texas-Red Channel 4: CY 5 Channel 5: QUASAR705, CY5.5 Channel 6: ATTO425 Channel 7: CY7 Channel 8: AF405

Thermal System

Control Mode	Temperature control mode
Temperature Indication Error	±0.1℃
Temperature Uniformity	±0.1℃
Temperature Control Range	4℃- 99℃
Avg Heating Rate	≥8℃/Sec
Max Heating Rate	≥10℃/Sec
Avg Cooling Rate	≥5℃/Sec
Max Cooling Rate	≥7℃/Sec
Hot-lid	Auto Hot-lid （Adjustable range 30℃ - 120℃/default 105℃)

Working Condition

Operating System	Windows 7/8/10/11
Software	Packaged project management
Power	850 W
Power Input	100 - 240 VAC, 50/60Hz
Size	208mm × 317mm × 243mm (W×D×H)
Weight	10kg
Interface	USB

Natch S Pro — Fully Automated Nucleic Acid Extraction System

Workflow

Features

Integrated all-in-one platform for seamless workflow The unified system integrates sample preparation, nucleic acid extraction, and subsequent processing in a single device, eliminating manual transfers and minimizing cross-contamination risks. 1. CO-RE technology for precise pipetting

Unique Compression-induced O-Ring Expansion (CO-RE) technology ensures precise tip at attachment and positioning.

2. Low temperature preservation module to ensure enzymatic activity

A low temperature module is equipped to prevent the reduction of enzyme activity

3. Independent waste liquid channel to prevent countertop contamination

The waste liquid channel is designed to work separately from the workstation, ensuring the cleanliness of the laboratory table

4. 96 HEAD, Greatly shorten nucleic acid extraction time

Full board extraction time is reduced to 2hours Detection efficiency increased to 3.5h to complete 96 tests

5. One-click automatic operation, no need to be on duty throughout the process

Interface operation is simplified, and the whole process of nucleic acid extraction can be automatically completed with one click

Specifications

Instrument Model	S-S14D
Sample Type	Serum, plasma, Whole blood
Technology Platforms	Advanced magnetic beads technology
Sample Throughput	576 tests/batch
Detection Time	Pooling test: 576 tests/4.5 hours; Individual test: 96 tests/3.5 hours
Sample Tube Spec.	Compatible with original sample tubes of all sizes
Pipetting Range	0.5-1000μL
Pipetting Performance	Pipetting volume 10μL, CV≤5%; 100μL, CV≤2%; 1000μL, CV≤1.5%
Pipetting Channel	8 independent channels, with dual liquid level detection, clot detection, air tightness detection, tip detection, dynamic positioning and other functions.
Liquid Level Detection	Dual detection technology of pressure and capacitance can identify and record abnormal suction and discharge process (empty suction, missing suction, less suction, clot blockage)
Extraction Principle	Pipetting, side magnetism
Magnetic Field Control	Permanent magnet mode, three-dimensional surround magnetic attraction technology
Tips Loading and Uploading	CO-RE technology automatic tip loading and uploading
Temperature Control Range	Low temperature module: 0-15℃ adjustable Heating module: 5-105℃ adjustable
Anti-contamination System	UV lamp function, independent waste liquid channel
Barcode Scanning	Sample automatic scanning and sampling system (supports multiple barcodes), scanning time ≤ 1s
Software System	Window 7, Window 10 (recommended)
Interface Type	USB interface, RS232C serial port, support LIS system
Operating Environment	Temperature: 15-30 ℃ Humidity: 15%-85% (indoor, no condensation)
Weight and Size	About 220Kg, 2619mm(L)903mm(H)1043.5mm(W)
Power Supply	Voltage: 115VAC/230VAC, ±10% Frequency: 50/60Hz
Certification	NMPA

Natch S Pro — Fully Automated Nucleic Acid Extraction System

Workflow

Features

1. CO-RE technology for precise pipetting

Unique Compression-induced O-Ring Expansion (CO-RE) technology ensures precise tip at attachment and positioning.

2. Low temperature preservation module to ensure enzymatic activity

A low temperature module is equipped to prevent the reduction of enzyme activity

3. Independent waste liquid channel to prevent countertop contamination

The waste liquid channel is designed to work separately from the workstation, ensuring the cleanliness of the laboratory table

4. 96 HEAD, Greatly shorten nucleic acid extraction time

Full board extraction time is reduced to 2hours Detection efficiency increased to 3.5h to complete 96 tests

5. One-click automatic operation, no need to be on duty throughout the process

Interface operation is simplified, and the whole process of nucleic acid extraction can be automatically completed with one click

Specifications

Instrument Model	S-S14A
Sample Type	Serum, plasma
Technology Platforms	Advanced magnetic beads technology
Sample Throughput	576 tests/batch (pooling test); 96 tests/batch (individual test)
Extraction Time	576 tests ≤ 3 hours; 96 tests ≤ 2.5 hours
Sample Tube Spec.	Compatible with original sample tubes of all sizes
Pipetting Range	0.5-1000μL
Pipetting Performance	Pipetting volume 10μL, CV≤5%; 100μL, CV≤2%; 1000μL, CV≤1.5%
Pipetting Channel	8 independent channels, with dual liquid level detection, clot detection, air tightness detection, tip detection, dynamic positioning and other functions.
Liquid Level Detection	Dual detection technology of pressure and capacitance can identify and record abnormal suction and discharge process (empty suction, missing suction, less suction, clot blockage)
Extraction Principle	Pipetting, side magnetism
Magnetic Field Control	Permanent magnet mode, three-dimensional surround magnetic attraction technology
Tips Loading and Uploading	CO-RE technology automatic tip loading and uploading
Temperature Control Range	Low temperature module: 0-15℃ adjustable Heating module: 5-105℃ adjustable
Anti-contamination System	UV lamp function, independent waste liquid channel
Barcode Scanning	Sample automatic scanning and sampling system (supports multiple barcodes), scanning time ≤ 1s
Software System	Window 7, Window 10 (recommended)
Interface Type	USB interface, RS232C serial port, support LIS system
Operating Environment	Temperature: 15-30 ℃ Humidity: 15%-85% (indoor, no condensation)
Weight and Size	About 150Kg, 1664mm(L)903mm(H)795mm(W)
Power Supply	Voltage: 115VAC/230VAC, ±10% Frequency: 50/60Hz
Certification	CE, NMPA

S3214E B19 – Human Parvovirus B19 DNA Nucleic Acid Diagnostic Kit

Other Infections

Brief

The Human Parvovirus B19 DNA Diagnostic Kit (PCR-Fluorescence Probing) is a real-time PCR test intended for the qualitative detection of nucleic acid from Human Parvovirus B19 in plasma, serum from individuals who are suspected of B19 infection.

Parameters

Product features	Parameter
Specimen Type	Plasma, serum
Extraction Platform	Advanced magnetic beads technology
Extraction Reagent	S1006E
PCR Instrument	MA6000, SLAN-96P, QuantStudio 5, ABI7500, Roche 480
Sensitivity	400 copies/mL
Spec.	24T, 48T
Qualification	CE

S3179E HAV – Hepatitis A Virus RNA Nucleic Acid Diagnostic Kit

Gastrointestinal Infections (GIIs)

Brief

The Hepatitis A Virus RNA Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing) is a Real-time PCR test intended for the qualitative detection of nucleic acid from HAV in plasma and faeces.

Parameters

Product features	Parameter
Specimen Type	Plasma
Extraction Platform	Advanced magnetic beads technology
Extraction Reagent	S1006E
PCR Instrument	MA6000, SLAN-96P, QuantStudio 5, ABI7500, Roche cobas 480, CFX96
Sensitivity	1000 copies/mL
Spec.	24T
Qualification	CE

SLAN-48S — Real-Time PCR Instrument

Brief

SLAN-48S, the avant-garde leader in real-time fluorescent quantitative PCR analysis, is designed for on-the-go testing. Its six independent modules with 8-channel system offer seamless multiplex testing, simplifying even the most complex procedures into effortless tasks. With a sleek and portable design that fits easily into your backpack, you are empowered to conduct molecular detection with unmatched ease and precision. Elevate your testing experience to a new level of convenience and efficiency today.

Manual Operation ＜ 1 min, Results in 30 mins

Revolutionary temperature control technology 1. Amplification takes only 30 minutes, approximately half the time of conventional PCR instruments. 2. It enables the rapid and accurate detection of gene expression variations as minimal as 2-fold.

Flexible and independent modules 1. Each module is equipped with integrated temperature control system and heat lid, allowing for immediate testing upon arrival. 2. It serves as a gradient fluorescence PCR system and can simultaneously set 6 temperature and time gradients to compare amplification effects and identify the optimal reaction conditions, aiding in reagent development.

Smart Portable Design 1. Weighing under 10 kg, the instrument is one-third the weight of conventional thermal cyclers and can be carried in a backpack for molecular detection. 2. The instrument is operational without calibration after relocation. 3. Compatible with outdoor mobile power supplies for mobile detection.

Interoperable Open Platform Compatible with various reagents, the device allows for customized experiments.

Eight-color fluorescence detection system Detects up to 8 targets per well, enhancing efficiency.

Specifications

Performance

Sample Capacity	48 Wells (6×8-well×0.2mL)
Parallel Experiment	6 reaction modules run up to 6 different experiments at the same time
Consumables	0.2mL PCR tubes, 4-tube strip
Light Source	High power Led (Maintenance-free)
Detector	High sensitivity photoelectric sensor
Dynamic Range	10⁰ - 10¹⁰
Sensitivity	1 copy
Quantitative Repeatability	CV＜2.00%
Correlation	\|r\|≥0.9990
Concentration Differentiation	2-fold
Sample Volume	15μL - 100μL
Probe/Dye	Channel 1: FAM, SYBR-Green Channel 2:VIC, HEX, JOE, TET Channel 3: ROX, Texas-Red Channel 4: CY 5 Channel 5: QUASAR705, CY5.5 Channel 6: ATTO425 Channel 7: CY7 Channel 8: AF405 *Channel 7 and Channel 8 can be customized according to user needs.

Thermal System

Control Mode	Fast/Standard
Temperature Indication Error	±0.1℃
Temperature Uniformity	≤0.1℃
Temperature Control Range	4℃- 99℃
Avg Heating Rate	≥8℃/Sec
Max Heating Rate	≥10℃/Sec
Avg Cooling Rate	≥6℃/Sec
Max Cooling Rate	≥8℃/Sec
Hot-lid	Auto Hot-lid （Adjustable range 30℃ - 120℃/default 105℃)

Working Condition

Operating System	Windows 7/8/10/11
Software	Packaged project management
Power	600 W
Power Input	100 - 240 VAC, 50/60Hz
Size	343mm×295mm×156mm(W×D×H)
Weight	9kg
Interface	USB

SNMC0021IR HPV G14 – High-risk Human Papillomavirus DNA (14 Genotypes) Diagnostic Kit

Reproductive Tract Infections

Brief

This High-risk HPV DNA (Genotype) Diagnostic Kit (PCR-Fluorescence Probing) is an in vitro nucleic acid amplification test for the detection of high-risk HPV (type 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68) present in exfoliated cells from females’ cervix. The test results can be used for identification of HPV genotypes.

Parameters

Product features	Parameter
Specimen Type	Exfoliated cells from females’ cervix
Technical Platform	One-tube fast release technology Advanced magnetic beads technology
Detection types	type 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68
Internal Control	β--globin gene
PCR Instrument	SLAN-96P, ABI 7500, Roche LC 480 and QuantStudio^TM 5 , Stratagene Mx3000P
Amplification Time	70 min
Sensitivity	400 copies/mL
Spec.	24T

This kit is intended solely for the Iranian market.

iPonatic III Pro — Portable Molecular Diagnostic System

mPOCT

Brief

To provide time-saving, labor-saving and safe solutions for efficient nucleic acid analysis is always the intention of research and development for Sansure iPonatic series product. The iPonatic III Pro combines the core technical advantages of the previous generations of iPonatic series products, integrates better fluid controlling, magnetic beads method for nucleic acid extraction and PCR process, to avoid the traditional PCR experimental process time-consuming, complex operation and other drawbacks. By truly realizing the "sample in, result out" fully automated gene detection, and with Sansure’s flexible and extended testing menu, iPonatic III Pro is the ultimate choice for efficient molecular diagnostics.

Features

Simplicity: Fully automated DNA/RNA extraction and detection to minimize manual labor
Precision: Features fast PCR with real-time data analysis for reliable results
Scalability: Manages up to 8 devices with iScreen, meeting diverse testing demands
Speed: Delivers results within approximately 1 hour, ensuring rapid TAT time
Compatibility: Processes various pathogens across different Viral Transport Media
Intelligence: Offers wireless LIS and IoT connectivity for advanced disease surveillance

Specifications

Parameter
Module	1 (up to 8, connected by iScreen)
Dimension	About 400mm * 141mm * 401mm (LWH)
Weight	About 9.9kg
Functions	Nucleic acid extraction, amplification & detection, data analysis
Sample process	Liquid transfer, heating and ultrasonic funciton (S-Q37A only) for DNA purification
Analysis	Support melting curve analysis
Channels	FAM, VIC, ROX, CY5
Maximum heating rate	10°C/sec
Maximum cooling rate	3°C/sec
Temperature accuracy	±0.5°C
Display	Built-in 7-inch high-definition touch screen
Communication	USB2.0, RJ45, Type-C, Wi-Fi, Bluetooth, IIS_LH7
Power supply
Input voltage	100~240 VAC
Power frequency	50/60 Hz
Rated power	140 VA
Environment Requirement
Operating temperature	10°C ~ 30°C
Operating humidity	20%RH ~ 85%RH, non-condensing
Barometric pressure	85.0 kPa ~ 106.0 kPa
Altitude	Less than 3,000 m
Transportation and storage	Environment temperature range: -20°C ~ 55°C Relative humidity range: ≤85%RH, non-condensing

Order Information

Category	Product Name	Cat. No.
Instrument	S-Q37A (with ultrasonic function)	S-Q37A
Instrument	S-Q37B (without ultrasonic function)	S-Q37B

Category	Reagent	Analytes	Cat. No.
Extraction Kit	Nucleic Acid Extraction-Purification Kit	/	S50016E-12A

PCR Kit	Respiratory	Six RP	Influenza A virus, Influenza B virus, Respiratory syncytial virus, Adenovirus, Human rhinovirus and Mycoplasma pneumonia	S3066E
		SARS-CoV-2/Flu/RSV	SARS-CoV-2, Influenza virus A/B (Flu) and Respiratory syncytial virus (RSV)	S3148E-12-P
		COVID	ORF1ab and N genes of novel coronavirus (2019-nCoV)	S3102E
		SARS-CoV-2/Flu A/B	SARS-CoV-2, Influenza A and Influenza B	S3113E-12-P
		MP	Mycoplasma pneumoniae	S3016E
	Reproductive Tract Infections	HPV13+2	Human papillomavirus(16, 18, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 66, 68)	S3057E
	Reproductive Tract Infections	MG/MH/TV	Mycoplasma genitalium, Mycoplasma hominis, and Trichomonas vaginalis	S3250E-12-P
	Gastrointestinal Infections	EV/EV71/CA16	Enterovirus, Coxsackievirus A16 and Enterovirus 71	S3053E
	Others	GBS	Group B streptococcus	S3056E
		DENV/ZIKV/CHIKV	Dengue virus (DENV), Zika virus (ZIKV), and Chikungunya virus (CHIKV) RNA	S3333E-12-P
		C.diff	Clostridium difficile	S3350E

Use scenarios

Hospital, Nursing Home, Airport, Cruise, CDC, Clinic, Lab, Pharmacy, etc.

*All use scenarios must comply with local regulations.

Product video

https://youtu.be/oGEpTLWrCIU?si=WUtry-NhRyFGeSup

S3055E BP – Bordetella Pertussis DNA Diagnostic Kit

Brief

Pertussis, also known as whooping cough, is a highly contagious respiratory infection caused by the bacterium Bordetella pertussis. Pertussis spreads easily from person to person mainly through droplets produced by coughing or sneezing. The disease is most dangerous in infants, and is a significant cause of disease and death in this age group.

Sansure kit is used to detect Bordetella pertussis DNA present in the nasopharyngeal swab specimens by applying PCR fluorescence probing technique. The detection result can be used as an aid in the diagnosis of bordetella pertussis.

Parameters

Product features	Parameter
Specimen Types	Nasopharyngeal swab
Technical Platform	Fast release technology Advanced magnetic beads technology
Anti-contamination system	UNG enzyme + dUTP system
Internal Control	Internal control plasmid
PCR Instruments	Mx3000P; ABI 7500; MA-6000; S-Q31A/S-Q31B; S-Q36A
Sensitivity	200 copies/mL
Obtained Certificates	NMPA, CE

Natch 16S — Nucleic Acid Extraction System

Specification

Instrument Model	Natch 16S
Extraction Technology	Magnetic bead technology, magnetic rod and tip comb method
Sample throughput	1 ~ 16
Sample type	Serum, plasma, throat swabs, anal swabs, feces, genital tract secretions, exfoliated cells, urine, sputum etc.
Working volume	30 ~ 1000μL
Magnetic Rod Quantity	16
Purification differences between wells	CV≤5%
Heating Temperature	From room temperature to 100 °C
Mixing mode	Tip comb moving up and down to mix
Extraction time	10 ~ 60 minutes/batch
Anti-contamination	Built-in UV lamp and air filtration system
Display	7-inch touch screen
Operation mode	Touch control
Internal Programs	30 Groups
Power supply	Input:100 ~ 240 V,50 ~ 60 Hz,2.0 A
Dimension (L×D×H)	220×440×425 mm
Weight	16kg
Interface	USB 2.0 (for data transfer)

Extraction kit components

Reagent Kit	Product Name	Spec.
S10016E	Nucleic Acid Extraction Purification Kit	64T
S50016E	Nucleic Acid Extraction Purification Kit	64T

Available projects

Sexually Transmitted Diseases : CT, NG, UU, HSV-2, HSV I/2 Women's Health : hrHPV and hrHPV genotyping Respiratory Tract Disease : 6RP, TB, MP, RSV, ADV, BP Gastrointestinal Diseases : HFMD Prenatal and Postnatal care : CMV, EBV Public Health : SARS-CoV-2, Influenza A/B, HINI, H7N9 Customerized Projects

S3174E HCoV-MERS – Human Coronavirus (MERS) Nucleic Acid Diagnostic Kit

Brief

The Human Coronavirus (MERS) is generally detectable in respiratory samples during the acute phase of infection. The Human Coronavirus (MERS) Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing) can qualitatively detect HCoV-MERS in sputum, alveolar lavage fluid, and throat swabs, the test results can be used to assist in the diagnosis of patients infected with HCoV-MERS, providing a molecular diagnostic basis for coronavirus MERS infection. The test results of this kit are for clinical reference only, and should not be used as the sole criterion for clinical diagnosis. It is recommended to conduct a comprehensive analysis of the condition based on the patient's clinical manifestations and other laboratory tests.

Parameters

Product features	Parameter
Covering Genes	MERS-CoV Orf1b
Specimen Types	Sputum, alveolar lavage fluid, throat swab
Technical Platform	One-tube fast release technology Advanced magnetic beads technology
Internal Control Gene	RNase P
Compatible Instruments	ABI 7500, Stratagene Mx3000P, SLAN®-96P, MA-6000, iPonatic S-Q36A/S-Q31A/S-Q31B
Sensitivity	500 copies/mL
Qualification	CE

S3104E 2019-nCoV (FDA EUA)Novel Coronavirus (2019-nCoV) Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing)

2019-nCoV (FDA EUA)

For in vitro diagnostic use only.

For emergency use only.

For Prescription Use only.

Rx only.

Brief

The Novel Coronavirus (2019-nCoV) Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing) is a real-time RT-PCR test intended for the qualitative detection of nucleic acid from SARSCoV-2 in nasopharyngeal swabs, oropharyngeal (throat) swabs, anterior nasal swabs, midturbinate swabs, nasal washes and nasal aspirates from individuals who are suspected of COVID-19 by their healthcare provider. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. §263a, that meet requirements to perform high complexity tests.

Results are for the identification of SARS-CoV-2 RNA. The SARS-CoV-2 RNA is generally detectable in respiratory specimens during the acute phase of infection. Positive results are indicative of the presence of SARS-CoV-2 RNA; clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status. Positive results do not rule out bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease.

Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for patient management decisions. Negative results must be combined with clinical observations, patient history, and epidemiological information.

Performance

One-tube/fast release technology
Simple operation process, less specialist training
Room temperature lysis, less contamination
Sampling types: nasopharyngeal swabs, oropharyngeal (throat) swabs, anterior nasal swabs, midturbinate swabs, nasal washes and nasal spirates
Internal control: human housekeeping gene RNase P

Parameters

Product features	Parameters
Specimen Type	Nasopharyngeal swabs, oropharyngeal (throat) swabs, anterior nasal swabs, midturbinate swabs, nasal washes and nasal spirates
Extraction Platform	Sample Release Reagent Qiagen QIAamp Viral RNA Mini Kit
Target Genes	SARS-CoV-2 ORF1ab, N gene
Internal Control	Rnase P gene
PCR Instrument	ABI 7500 Real-Time PCR System
LoD	200 copies/mL
Spec.	24T, 48T
Qualification	FDA EUA

Notes

This test has not been FDA cleared or approved;
This test has been authorized by FDA under an EUA for use by authorized laboratories;
This test has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens; and
This test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of the emergency use of in vitro diagnostic tests for detection and/or diagnosis of COVID-19 under section 564(b)(1) of the Act, 21 U.S.C. § 360bbb- 3(b)(1), unless the authorization is terminated or revoked sooner.

S3353E Flu A/B – Influenza A/B Virus Nucleic Acid Diagnostic Kit

Brief

Influenza Virus is a kind of RNA virus in the Orthomyxoviridae family which leading to human and animal influenza. It causes acute upper respiratory tract infection, spreads rapidly through the air and has periodic pandemics around the world. Human influenza virus are influenza pathogens which can be classified into three types, namely A, B and C. Among them, influenza A is the most harmful, while influenza B and influenza C have weak pathogenicity and are not easy to mutate.

The diagnostic Kit is intended for detection of the Influenza A and Influenza B in oropharyngeal swab from individuals. The test results can be used for the auxiliary diagnosis of respiratory Influenza A/B Virus infection and provide molecular diagnostic basis for Influenza A/B Virus infection.

Parameters

Product features	Parameter
Covering pathogens	Influenza A and Influenza B
Specimen Types	Oropharyngeal swab
Technical Platform	One-tube fast release technology Advanced magnetic beads technology
Compatible Instrument	ABI 7500; MA-6000; SLAN®-96P; QuantGene 9600; iPonatic S-Q31A/S-Q31B
Sensitivity	200 copies/mL
Spec.	48T, 24-P
Qualification	CE

S3363E-12-P TB and RFP – Mycobacterium Tuberculosis Nucleic Acid and Rifampicin Resistance Fluorescence Diagnostic Kit

Brief

Mycobacterium tuberculosis (M. tuberculosis) is the pathogen causing tuberculosis, which can invade all organs of the whole body, and pulmonary tuberculosis caused by pulmonary involvement is the most common. Early diagnosis and treatment are crucial measures to effectively control the spread of tuberculosis.

Due to the abuse of antibiotics or the insufficient course of drugs of patients, the sensitivity of patients to drugs weakens or even disappears, resulting in the decreasing or ineffective effect of drugs on pulmonary tuberculosis. According to the types of anti-tuberculosis drugs, drug-resistant tuberculosis can be divided into monoresistance pulmonary tuberculosis, polyresistance pulmonary tuberculosis, multidrug resistance pulmonary tuberculosis and extensively drug-resistant pulmonary tuberculosis. Rifampicin is one of the first-line drugs for the treatment of pulmonary tuberculosis.

The Mycobacterium Tuberculosis and Rifampicin Resistance Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing) is a real-time polymerase chain reaction test kit intended for the qualitative detection of the nucleic acid of mycobacterium tuberculosis and rifampicin resistance mutations in human sputum samples. The test results can be used to assist in the diagnosis of TB patients and patients with an increased risk of RFP drug-resistant TB, providing a molecular diagnosis basis for infected patients.

Parameters

Product features	Parameter
Specimen Type	Sputum
Technical Platform	One-tube fast release technology
PCR Instruments	iPonatic Ⅲ (S-Q36A)
Internal Control	RNase P
Limit of detection	Mycobacterium tuberculosis 1,000 Bacteria/mL; Rifampicin resistance 10,000 Bacteria/mL

The kit is registered in Indonesia.

Sample Storage Reagent

Brief

The Sample Storage Reagent is intended for preservation and transportation of cells from human body.

The Sample Storage Reagent can protect the stability of virus and intracellular nucleic acid in clinical samples in a short term and is beneficial to the transport of clinical samples.

Kit Components

Cat. No.	Product Description	Package	Registration
X1001E	Sample Storage Reagent specimen type:Cervical exfoliated cell	1T/24T	СЕ NMPA
X1006E	Sample Storage Reagent specimen type:Cervical exfoliated cell	25T/50T/100T/200T/300T/400/500T	CE NMPA
X1011E	Sample Storage Reagent XI specimen types:oral and nasopharyngeal swabs	24T/48T/96T	CE NMPA
N101E	Urine Sample Collector	1T/40T	CE NMPA

S3108E HPV G23 – Human Papillomavirus DNA (23 genotypes) Diagnostic Kit

HPV Infections

Brief

Human Papillomavirus DNA (23 genotypes) Diagnostic Kit (PCR-Fluorescence Probing) is an in vitro nucleic acid amplification test for the detection of high-risk HPV (Type 6, 11, 16, 18, 26, 31, 33, 35, 39, 42, 43, 45, 51, 52, 53, 56, 58, 59, 66, 68, 73, 81, 82) present in exfoliated cells from females’ cervix. The test results can be used for identification of HPV genotypes.

Parameters

Product features	Parameter
Specimen Type	Exfoliated cells from females’ cervix
Technical Platform	One-tube fast release technology Advanced magnetic beads technology
Detection types	Type 6, 11, 16, 18, 26, 31, 33, 35, 39, 42, 43, 45, 51, 52, 53, 56, 58, 59, 66, 68, 73, 81, 82
Internal Control	β--globin gene
PCR Instrument	Stratagene ABI7500, Life Technologies QuantStudio^TM5 and SLAN-96P
Amplification Time	70 min
Sensitivity	400 copies/mL
Spec.	24T/48T
Qualification	CE

Order Information

Ref. No.	Product Name	Spec.
S3108E	Human Papillomavirus DNA (23 genotypes) Diagnostic Kit (PCR-Fluorescence Probing)	24T, 48T/Kit
S1013E	Sample Release Reagent	48T/Kit
S10016E	Nucleic Acid Extraction-Purification Kit	24T, 48T, 96T/Kit

iPonatic III — Portable Molecular Workstation

mPOCT

Brief

iPonatic III - Portable Molecular Workstation is a new member of Sansure's iPonatic series, optimizing molecular diagnostics with its advanced capabilities. With its cutting-edge technology, iPonatic III ushers in a new "digital and intelligent" era of molecular diagnostics, empowering healthcare professionals and providing rapid and accurate results.

Features

Extensive test menu to better serve healthcare community
Sample in,result out: results can be delivered in 15-45 minutes
Flexible wireless connection: up to 8 units can be wirelessly connected to satisfy random access; LIS compatible
Built-in touchscreen in compact body design to fit different scenarios
Accurate PCR results to support precise diagnosis
Pre-packaged kits and uniquely designed carrier set for easier handling minimal hands-on time
User friendly software with intuitive SanUl can provide automated analysis and clear result display

Parameters

Model	S-Q36A
Dimension	391 mm×140 mm×368 mm (L×W×H)
Weight	About 7.2kg
Channels	FAM, VIC/HEX, ROX/Texas Red, CY5
Duration	15 - 45min (SARS-CoV-2)
LOD	200 copies/mL (SARS-CoV-2)
Maximum heating rate	≥10℃/sec
Maximum cooling rate	≥3℃/sec
Temperature accuracy	±0.5°C
Functions	Nucleic acid extraction, amplification detection, data analysis
Display	Built-in 7-inch high-definition touch screen, 12.1-inch smart screen (optional)
Interfaces/communication	USB2.0, RJ45, Type-C, WI-FI, Bluetooth, LIS_LH7
Input voltag	100-240 VAC
Power frequency	50/60Hz
Rated power	160VA
Temperature	Operating conditions:10°C- 30°C Transportation and storage: -40°C- 55°C
Humidity	Operating conditions: 30% - 80%, non-condensing Transportation and storage: ≤ 93%, non-condensing
Barometric pressure	85.0kPa - 106.0k Pa
Altitude	Less than 3,000 m
Qualification	CE

Test menu

RTI: SARS-CoV-2 (ORF1ab, N gene) SARS-CoV-2 (ORF1ab, N gene, E gene) SARS-CoV-2/Flu A/Flu B SARS-CoV-2/Flu/RSV Six Respiratory Pathogens (Flu A/Flu B/RSV/AdV/HRV/MP) Acinetobacter baumannii and Canidia albican (AB/CA) Flu A/Flu B Mycoplasma Pneumoniae (MP) Mycobacterium Tuberculosis (TB) Bordetella Pertussis (BP) Respiratory Syncytial Virus (RSV) Streptococcus Pneumoniae (SP) Carbapenemase Gene (KPC) MERS Legionella pneumophila (Lp) Adenovirus (AdV) STI & HPV: HPV 13+2 (Identifies HPV 16 and HPV 18, reports 13 other high risk types in pooled results) HPV 15 HR (Reports 15 high risk HPV types in pooled results) HPV 16&18 HPV 6&11 HSV-2 HSV-1&2 Mycoplasma Genitalium/Mycoplasma Hominis/Trichomonas Vaginalis (MG/MH/TV) Neisseria Gonorrhoeae (NG) Ureaplasma Urealyticum (UU) Mycoplasma Genitalium (MG) Chlamydia Trachomatis/Ureaplasma Urealyticum/Neisseria Gonorrhoeae(CT/UU/NG) Other infections: Epstein-Barr Virus (EBV) Group B Streptococcus (GBS) Toxigenic Clostridium difficile (CD) * Monkeypox Virus (MPXV) *

Use scenarios

Medical laboratories, emergency rooms, fever clinics, remote areas, CDCs, airports, customs, etc.

*All use scenarios must comply with local regulations.

S3046E HIV-1 – Human Immunodeficiency Virus Type 1 RNA Quantitative Fluorescence Diagnostic Kit

Brief

Human Immunodeficiency Virus Type 1 RNA Quantitative Fluorescence Diagnostic Kit (PCR-Fluorescence probing) is intended for quantitative detection of the HIV-1 Virus RNA in human EDTA plasma specimens and used as an aid for diagnosis of HIV infection or carrier.
Test results shall not be used as the only indicator for clinical diagnosis, and a comprehensive analysis of the condition must be conducted in combination with the patient's clinical manifestations and other laboratory tests.
The kit MUST NOT be used for blood screening.
For in vitro diagnostic use only. For professional use only.

Features

Patented Modified-Capture Probe Assay – Using exclusive modified super-paramagnetic nano-beads to adsorb RNA in the sample; – Heating free: Innovative lysis solution, no heating, less aerosol contamination; – Single wash step: Unique combination of inorganic and organic solutions for reduced handling steps and reduced HIV-1 RNA loss. Dual Targets The LTR and pol gene regions were selected as targets for HIV detection to reduce the risk of false-negative results and improve assay sensitivity. High Sensitivity The limit of detection was 25 IU/mL, meeting international guidelines for HIV-1 detection. Internal Control The use of an internal control during extraction and amplification ensures process validity and reduces the likelihood of false-negative results.

Parameters

Items	Parameter
Specimen Type	Plasma
Extraction Platform	Advanced magnetic beads technology
Group	HIV-1 Group M, O and N
Internal Control	Pseudoviruses
PCR Instrument	SLAN-96P, ABI7500, Roche cobas 480
Sensitivity	25 IU/mL
Linear range	50—1.0E+08 IU/mL
Spec.	48T
Qualification	CE

ORDER INFORMATION

Cat. No.	Product Name	Spec.
S3046E	Human Immunodeficiency Virus Type 1 RNA Quantitative Fluorescence Diagnostic Kit (PCR-Fluorescence Probing)	48T
S1001E	Nucleic Acid (RNA) Extraction or Purification Kit (Magnetic beads method)	24T

Related Instruments

S3016E MP – Mycoplasma Pneumoniae DNA Fluorescence Diagnostic Kit

Brief

Mycoplasma pneumoniae (MP) is a pathogenic microorganism between bacteria and virus. It is mainly transmitted through buccal and nasal mucus by the air causing respiratory diseases, with the highest incidence in children and adolescents. Respiratory infection has the manifestations of pharyngitis and bronchitis, with a few cases causing infection to the lung. Recently, incidence among infants and children is increasing, therefore, early diagnosis and treatment can decrease the exacerbation of acute pneumonia in children. The development of molecular biology also draws more attention to the fluorescence quantitative PCR technology for the detection of MP-DNA. This diagnostic kit is an in vitro nucleic acid amplification test for the detection of mycoplasma pneumoniae DNA in humansputum and throat swab. It is intended for use as an aid in the diagnosis of an MP infection and providing a molecular-diagnostics-based solution.

Parameters

Product features	Parameter
Specimen Type	Sputum and throat swab
Extraction Platform	One-tube fast release technology
Internal Control	cloning plasmid containing the target gene fragment
PCR Instrument	ABI 7500, SLAN-96P,MA-6000, Roche LightCycler 480, iPonatic S-Q31A&B,S-Q36A
Sensitivity	400 copies/mL
Spec.	48T, 12-P
Qualification	CE

S3066E 6RP – Six Respiratory Pathogens Nucleic Acid Diagnostic Kit

Brief

Respiratory infections are classified into the upper respiratory tract infections and lower respiratory tract infections. It refer to the pathogens that infect the nose, throat, trachea, bronchi or lungs, which principally cause diseases of tissues and organs outside the respiratory tract, manifested by fever, sore throat, cough, headache and other symptoms. The respiratory tract pathogen has the characteristics of strong infectivity, rapid spread, short incubation period and acute onset, etc. which seriously harm human health. After respiratory infection, symptoms are mostly similar. Sansure six respiratory pathogens joint detection kits can help doctors make differential diagnosis, accurately detect the pathogens that cause symptoms, and formulate treatment plans.

Performance

High sensitivity: Super-cis-nanometer magnetic bead technology; can achieve 500copies/mL
Accurate identification: One test presented six results ; accurate guidance for rational clinical drug use
Whole-process monitoring: Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) human housekeeping gene as internal standard; Monitor the whole process of sampling, nucleic acid extraction and amplification

Parameters

Product features	Parameter
Specimen Type	Nasopharyngeal swabs
Extraction Platform	Advanced magnetic beads technology
Internal Control	lentivirus particles（GAPDH）
PCR Instrument	SLAN-96P, ABI7500, S-Q36A
Sensitivity	Influenza A virus: 2.0 TCID₅₀/mL Influenza B virus: 2.0 TCID₅₀/mL Respiratory syncytial virus: 500.0 copies/mL Adenovirus: 500.0 copies/mL Mycoplasma pneumonia: 500.0 copies/mL Human rhinovirus: 500.0 copies/mL
Spec.	24T, 12P
Qualification	CE

S3334E AdV – Adenovirus Nucleic Acid Diagnostic Kit

Brief

Acute infectious disease caused by adenovirus, easily affects the mucous membranes of the respiratory and digestive tracts, the conjunctiva of the eyes, the urinary tract and the lymph nodes. The main manifestation is an acute upper respiratory tract infection. The population is generally susceptible, mostly the children. Infants are susceptible to adenovirus pneumonia, which is severe and has a high mortality rate. The source of infection is the patient and the latent infected person. The virus is excreted from the respiratory tract and conjunctival secretions, feces and urine, and is transmitted by airborne droplets, close contact and the feces-oral route. The Adenovirus Nucleic Acid Diagnostic Kit is used for nucleic acid testing of adenovirus in patients suspected of being adenovirus infections (e.g., fever, cough, wheezing, dyspnea, bronchopneumonia, upper respiratory tract infections, lung infections, etc.) or related close contacts, and the results can be used to assist in the diagnosis of adenovirus infection and provide a molecular diagnostic basis for adenovirus infection.

Features

High sensitivity: Detection sensitivity reaches 200 copies/mL.
Quick and easy: Perfectly match Sansure's one-tube fast Sample Release Reagent, easy to operate.
IC monitoring: IC(Internal Control) monitoring test process to avoid false negative results.

Parameters

Items	Parameter
Specimen Type	Throat swab
Extraction Platform	One-tube fast release technology Advanced magnetic beads technology
Anti-contamination system	UNG enzyme + dUTP system
PCR Instrument	ABI 7500; MA-6000; SLAN-96P; QuantStudio 5; iPonatic S-Q31A&B; S-Q36A
Sensitivity	200 copies/mL
Qualification	NMPA, CE

S3018E TB – Mycobacterium Tuberculosis DNA Fluorescence Diagnostic Kit

Brief

Mycobacterium tuberculosis virus (TB) is a pathogenic bacterium that causes tuberculosis. It is likely to infect all human tissues and organs, especially the lungs to cause pulmonary tuberculosis. Early diagnosis and treatment are important for effective control of tuberculosis. In recent years, with the development of molecular biology, nucleic acid fluorescence quantitative PCR method based on the mycobacterium tuberculosis nucleic acid has drawn more and more attention from researchers.

Parameters

Product features	Parameter
Specimen Type	Human sputum
Extraction Platform	One-tube fast release technology
Internal Control	Cloning plasmid, without TB target sequence
PCR Instrument	ABI 7500, SLAN-96P,MA-6000, Stratagene Mx3000P, iPonatic S-Q31A&B,S-Q36A
Sensitivity	1 bacterium/mL
Spec.	48T, 12-P
Qualification	CE

S3310E 6LRP – Six Respiratory Pathogens Multiplex Nucleic Acid Diagnostic Kit

Brief

Lower respiratory infections (LRP) remained the world’s most deadly communicable disease, ranked as the 4th leading cause of death. In 2019 it claimed 2.6 million lives. Diseases of the lower respiratory tract include acute tracheitis, bronchitis, pneumonia, chronic bronchitis, chronic obstructive pulmonary disease, bronchiectasis, etc. They are caused by microbial infections such as viruses, bacteria, mycoplasma, chlamydia and legionella. Bacteria are the main pathogens of lower respiratory tract infections, with a wide variety of pathogens and complex clinical presentations. Due to the long detection period and low positive detection rate of traditional pathogenic tests, over 62% of adults with community-acquired pneumonia have no pathogenic basis. Failure to identify the cause quickly can delay treatment, exacerbate the disease and lead to death, and increase the development of antibiotic resistance.

Features

Highly efficient identification and rapid diagnosis: Six common bacteria of lower respiratory tract infections can be detected in one tube; a batch of 94 sample tests can finish in 100 minutes.
Accurate and reliable, high detection rate: sensitive and specific, unaffected by antibacterial drugs, full internal control monitoring to avoid false negatives, UDG enzyme + dUTP anti- contamination measures to reduce false positives.
Easy to operate and adaptable: automatic instruments are available, and the results can be intelligently analyzed by conventional fluorescent PCR instruments to meet the needs of medical laboratories , clinical Institutions, emergency and primary care etc.

Parameters

Items	Parameter
Specimen Type	Sputum
Extraction Platform	Advanced magnetic beads technology
Internal Control	Plasmid
PCR Instrument	Thermofisher QuantStudio™ 5 and SLAN-96P
Sensitivity	15 CFU/mL (Streptococcus pneumoniae) 340 CFU/mL (Legionella pneumophila) 625 CFU/mL (Haemophilus influenzae) 675 CFU/mL (Pseudomonas aeruginosa) 900 CFU/mL (Klebsiella pneumoniae) 2875 CFU/mL (Staphylococcus aureus)
Qualification	NMPA, CE

S3352E MPXV – Monkeypox virus Nucleic Acid Diagnostic Kit

Other Infections

Brief

Monkeypox is a disease of global public health importance as it not only affects countries in west and central Africa, but the rest of the world. Human-to-human transmission can result from close contact with respiratory secretions, skin lesions of an infected person or recently contaminated objects. Transmission via droplet respiratory particles usually requires prolonged face-to-face contact, which puts health workers, household members and other close contacts of active cases at greater risk. WHO recommends polymerase chain reaction (PCR) is the preferred laboratory test given its accuracy and sensitivity.

Performance

Test time ≤ 30 min
Sensitivity: 200 copies/mL
Suitable for PCR and iPonatic

Parameters

Items	Parameters
Specimen Type	Vesicles or pustules, nasopharyngeal swab, oropharyngeal swab, serum, whole blood
Extraction Platform	One-tube fast release technology Advanced magnetic beads technology
Internal Control	Human gene
PCR Instrument	ABI 7500, QuantStudio™ 5, LightCycler 480, MA-6000, SLAN-96P, QuantGene 9600, Portable Molecule Workstation S-Q31A&B, Portable Molecular Workstation S-Q36A
Sensitivity	200 copies/mL
Spec.	48 T, 12-P
Qualification	CE

C004E BCI – Nucleic Acid Test Kit for HBV, HCV, HIV (Type1+2)

Brief

The Nucleic Acid Test Kit for HBV, HCV, HIV (Type1+2) (Real-time PCR) is intended for qualitative detection and screen the Hepatitis B Virus (HBV) DNA, Hepatitis C Virus (HCV) RNA, Human Immunodeficiency Virus Type 1 (HIV-1) RNA and Human Immunodeficiency Virus Type 2 (HIV-2) RNA, in plasma and serum samples from individual human donors. Plasma and serum from all donors may be screened as individual samples. For donations, may be tested individually or be tested in pools comprised of an equal quantity of six samples. For in vitro diagnostic use only. For professional use only.

Advantages

High sensitivity

HBV 2.41 IU/mL
HCV 12.38 IU/mL
HIV-1 31.68 IU/mL
HIV-2 48.34 IU/mL

High efficiency

576 tests/ ~5h（pooling）
96 tests / ~4.5h（single)

Complete subtypes coverage

HBV genotypes A-H
HCV genotypes 1-6
HIV-1 group M/N/O
HIV-2

Multiple results in one test

4 tests in one test
Direct discriminative positive results

Automated detection

Extraction and amplification process/li>
Fully automated extraction and amplification/li>

Cost and space savings

One extractor + one amplifier
Less consumable material consumption

Parameters

Items	C004E
Product Name	Nucleic Acid Test Kit for HBV, HCV, HIV (Type1+2) (Real-time PCR)
Package Specification	96 tests/kit
Amplification	Multiplex real-time PCR
Extraction	Magnetic bead method
Sample type	Plasma, Serum
Sample Volume	960μL
LoD (Individual testing)	HBV 2.41 IU/mL; HCV 12.38 IU/mL HIV-1 31.68 IU/mL; HIV-2 48.34 IU/mL
Storage and Validity	Amplification kit: < −15°C, 12months; Extraction kit: 2 – 8°C, 12 months
Qualification	CE

Related Instruments

iPonatic II— Portable Molecule Workstation

Brief

Innovations in molecular assays—especially on the point-of-care testing (POCT) front—have spread this testing from molecular diagnostics laboratories into clinical microbiology laboratories—and now into general laboratories and even clinics and exam rooms.^[1] Access to sensitive and rapid infectious disease diagnostic assays is essential for accurate diagnosis, effective treatment, and timely infection control, making POCT vital to reducing TAT. With novel POCT on the horizon, future studies are warranted to determine cost savings, antimicrobial usage, TAT, patient impact, and how to best implement in non-microbiology clinical laboratories and clinics.^[2] Sansure iPonatic (Portable Molecule Workstation) aims to innovate traditional diagnostic mode and assist precision diagnosis. It can provide quickly and convenient diagnosis experience for clinical emergency, health management, military safety, biological emergency and other applications.

Core technologies

Rapid nucleic acid lysis at room temperature within 1 minute
Ultra fast amplification system in 8-45 minutes
Integrated automatic data analysis software
Results immediately printed by built-in printer

Performance

Diagnostic results consistent with international mainstream PCR instruments

Parameters

Model	S-Q31A		S-Q31B
Detection platform	Real-time PCR
Detection module	1 amplification module		4 amplification modules
Temperature control	Liquid metal coated ceramic heating / Air cooling technology
Heating rate	≥6.0℃ /s (from 50℃ to 95℃ )
Cooling rate	≥2.0℃ /s (from 95℃ to 50℃ )
Excitation light source	LED
Detector	High sensitivity photodiode
Applicable dyes	FAM	VIC	ROX	CY5
Sensitivity	Can detect single copy gene
Electrical specification	AC 100-200V 50/60Hz
Dimension	230×284×376 mm (L×W×H)		336.5 × 280 × 435 mm (L×W×H)
Weight	9.7Kg		13Kg
Qualification	CE

Test menu

Respiratory Infections : SARS-CoV-2, SARS-CoV-2/FluA/B, MP, ADV, BP.... HPV Infections : HrHPV, HPV 13+2, HPV 16/18, HPV 6/11.... Children's health : EBV, HCMV.... STIs : CT/UU/NG, CT, UU, NG, HSV-2.... Other test projects are under development

References

[1]. Kozel TR, Burnham-Marusich AR. Point-of-care testing for infectious diseases: Past, present, and future. J Clin Microbiol 2017;55:2313-20.

[2]. Paige M.K. Larkin, Omai B. Garner. Molecular Point-of-Care Testing in Clinical Laboratories Laboratorians can lead a new era in rapid testing with expertise in quality control and result interpretation. Clinical Laboratory News. JUL.1.2020

View options

SLAN-96P — Real-Time PCR System

Features

Precise Temperature Control System: 1. The SLAN system adopts Peltier technology which can accurately and quickly control increases and decreases of temperature with a precision of ±0.1℃ and features long service life, no noise and no pollution, etc.; 2. Multiple-point temperature control technology ensures the uniformity between different wells. The temperature correction technology guarantees the accuracy of temperature and thus ensures the accuracy of assay result; 3. PCR tube temperature-control technology guarantees the accuracy of actual temperature of reagent in the tube and enables the SLAN to easily adjust for different reactions using different volumes. Sensitive Photoelectric Detection System 1. High sensitivity photoelectric detector with no background noise which is fast and stable; 2. Lifetime maintenance-free ultra-bright LED cold light source with a large signal value and high stability; 3. Unique optical fiber conduction technology that greatly improves fluorescence collection efficiency and avoids fluorescence interference between neighboring tubes; 4. The system automatically selects best gain value for each tube without the need for user configuration. The SLAN^®has an extremely broad measuring range for fluorescence; 5. Extremely high detection sensitivity with an extremely low fluorescence background value. It's not necessary for users to make optical correction or background correction.

SLAN-96P Multi-tasking Software Interface (analysis screen)

Unique Electronic Automatic Hot Lid System 1. Flexible heating technology ensures uniform hot lid temperature; 2. The electronic automatic hot lid has an adjustment function for different 0.2ml reaction tubes to ensure even tube pressure; 3. Once the assay starts, the hot lid has automatic locking function to prevent assay failure following accidental opening. Other functions

· Power-off protection	· Automatic saving result	· Export of result
· Real-time data display	· Quantitative and qualitative analysis	· File encryption
· Automatic baseline optimization	· Digital filtering	· Search function
· Report sheet print and edit	· Melt curve function

Specifications

Product model	SLAN-96P
Sample capacity	96 wells (dual 48/48 reaction module)
Sample size	15-50mL
Consumable	0.2mL PCR tubes, 8-tube strips, 48-well plates
Parallel running mode	Dual reaction blocks/running 2 tests independently
Temperature range	4-99°C
Max ramp rate	4.0°C/sec
Temperature accuracy	±0.1°C
Temperature uniformity	±0.1°C
Thermal cycling system	Peltier-based system
Temperature control mode	Tube control/block control
Light Source	LED (maintenance-free)
Detector	High sensitivity photoelectric sensor
Sensitivity	1 copy
Linearity range	10⁰-10¹⁰
Resolution	Can discriminate between 1000 copies and 2000 copies
Excitation	CH1 470nm CH2 530nm CH3 580nm CH4 630nm CH5/CH6 custom-made
Emission	CH1 510nm CH2 565nm CH3 620nm CH4 665nm CH5/CH6 custom-made
Dyes and probes	CH1 FAMTM /SYBRGreen® CH2 VIC®/HEX/J0ETM /TET CH3 ROX/TexasRed® CH4 CY5TM
Hot-lid	30°C~108°C (default105°C, adjustable) electronic automatic hot-lid
Power supply	230VAC, 50Hz
Power consumption	850VA
Dimensions	380mm x 520mm x 250mm (WxDxH)
Weight	18Kg
Communication	RS232, USB
Qualification	CE

Natch 48 — Nucleic Acid Extraction System

Extremely simple workflow

Specifications

Instrument model	Natch 24/48/96
Sample type	Serum, plasma, whole blood, secretions, exfoliated cells, tisues, throat swabs, anal swabs, urine, feces, etc.
Extraction technology	Advanced magnetic beads technology
Sample type Volume	1-96 tests/batch
Extraction Time	10-60 minutes each batch
Working volume	30-2000uL
Recovery rate of magnetic beads	＞95%
Blending mode	Vortex omnidirectional liquid mixing
Temperature control range	Adjustable from roomtemperature to 125℃
Operation	7-inch touch screen
Storage	Up to 120 groups of programs can be used.
Size and weight	655x655x520 mm (L x W x H), weight: 65kg
Qualification	CE

Extraction kit components

Reagent Kit	Product Name	Spec.
S10012E	Nucleic Acid (DNA/RNA) Extraction or Purification Kit (Magnetic beads method)	48A/48B
S10013E	Nucleic acid extraction (DNA/RNA) or purification kit (Magnetic beads method)	24T/48T
S10016E	Nucleic Acid Extraction-Purification Kit (Magnetic beads method)	24T/48T/96T
S50016E	Nucleic Acid Extraction-Purification Kit (Magnetic beads method)	48T/96T/24T/ 32T/64T

Available projects

Natch CS2 — Fully Automated Nucleic Acid Extraction System

Extremely simple workflow

Features

1. Efficient anti-contamination

Well-organized countertop layout
Sample area is separated from clean area
Effective UV decontamination
Anti-contanmination function of moving path

2. Super magnetic, effective adsorption

Super 3-D magnetic adhesion technology
Permanent magnetic mode
117 magnetic racks, 4 magnetic bars in each well

3. Excellent sample addition function

Automatic liquid level detection
Clot detection
Tip detection
Air-prof detection

4. Easy-to-use software

Preset programs, one-key selection
Prompt the placement of reagents
Display the status of reagents and consumables
Real-time display of remaining time
Show real-time experimental procedures
Permits LIS compatibility

Specifications

Instrument model	S-S13A
Sample type	Serum, plasma, whole blood, secretions, exfoliated cells, tissues, nasopharyngeal swab, oropharyngeal swab, urine, feces, etc.
Sample tube specifications	Compatible with various original sample tubes
Extraction Principle	one-tube fast release technology (OT) Advanced magnetic beads technology (MB)
Sample type Volume	OT: 1-96 tests/batch; MB: 1-96 tests/batch
Extraction Time	OT of 96 tests ≤ 30 minutes; MB of 96 tests ≤ 90 minutes
Pipetting range	10~1000 μL
Level detection	Pressure detection / capacitance detection, automatic detection of liquid level
Clot detection	Pressure detection, automatic detection of liquid aspiration and liquid clogging
Sample loading function	Automatic liquid level detection Clot detection Tips detection Air-prof detection
Magnetic field control	Permanent magnet mode Patented design Super 3-D magnetic adhesion technology
Blending mode	Vortex omnidirectional liquid mixing
Temperature control range	Adjustable from room temperature to 100℃
UV disinfection	Timed opening and closing
Barcode Scanning	Sample scanning system Supported multiple barcodes
Language	Simplified Chinese / English
Display Method	10.4 inches touch screen
Communication Interface	USB, RS232, network ports, HDMI
Dimensions and Weight	1320×850×1600mm (LxWxH), weight: 350Kg
Power supply	Input: AC 100-240V 50/60Hz 350 VA
Qualification	CE

Extraction kit components

Cat. No.	Product Description	Package	Registration
S100IE	Nucleic Acid (RNA) Extraction or Purification Kit (Magnetic beads method) Specimen types: Serum or plasma	24T/48A/48B/64T	CE NMPA
S1004E	Red Blood Cell Lysis Buffer	48T	CE NMPA
S1006E	Multi-type Sample DNA/RNA Extraction–Purification Kit (Magnetic beads method) Specimen types: serum, plasma, throat swab, genital secretion, cervical exfoliated cells	24T/48T/96T	CE NMPA
S1001E	Nucleic acid extraction (DNA/RNA) or purification kit (Magnetic beads method) Specimen types: throat swab, herpetic fluid, anal swab, feces, etc	24T/48T	CE NMPA
S10012E	Nucleic acid extraction (DNA) or purification kit (Magnetic beads method) Specimen types: Serum or plasma	48T/96T/48A/48B	CE NMPA
S10013E	Nucleic acid extraction (DNA/RNA) or purification kit (Magnetic beads method) Specimen types: Serum or plasma	24T/48T/48A/48B	CE NMPA
S10016E	Nucleic Acid Extraction–Purification Kit Specimen types: pharyngeal swabs, nasopharyngeal swabs, alveolar lavage fluid, sputum, saliva, plasma, serum, stool and anal swabs Specifications may vary depending on the extraction instruments	24T/48T/96T/24A/24B/ 48A/48B/48C/64T/96A	CE NMPA
S50016E	Nucleic Acid Extraction-Purification Kit Specimen types:pharyngeal swabs,nasopharyngeal swabs,oliveolar lavage uid sputum,saliva,plasma,serum,stool,oral swabs and exfoliated cells from females’ cervix,etc. Specifications may vary depending on the extraction instruments	48T/96T/12A/24A/24B/ 32A/32T/32S/48A/48B/ 48C/64A/64T/96A	CE NMPA
S5006E	Nucleic Acid Extraction-Purification Kit V–VI Specimen types:whole blood,serum,plasma.	48T/48A/48B/64T	CE
S5007E	Nucleic Acid Extraction-Purification Kit V–VII Specimen types:cervical swab,opharyngeal swab,nasopharyngeal swabs,anal swab,rectal and vaginal swabs.	48T/96T/48A/64T/96A	CE

Available projects

Hepatitis and AIDS : HBV, HCV, HIV Sexually Transmitted Diseases : CT, NG, UU, HSV-2, HSV I/2 Women's Health : hrHPV and hrHPV genotyping Respiratory Tract Disease : 6RP, TB, MP, RSV, ADV, BP Gastrointestinal Diseases : HFMD Prenatal and Postnatal care : CMV, EBV Public Health : SARS-CoV-2, Influenza A/B, HINI, H7N9 Customerized Projects

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S1006E Multi-type Sample DNA/RNA Extraction-Purification Kit
DNA/RNA Extraction Reagents

Brief
Multi-type Sample DNA/RNA Extraction-Purification Kit (Suprall extraction reagent) is an innovative product based on Sansure advanced magnetic beads technology platform , which can accomplish the unified extraction of nucleic acids in various gene detection applications and samples to provide comprehensive solutions for nucleic acid extraction , can be applied in infectious disease diagnosis, genetic disease screening, birth defect prevention, tumor screening, individualized diagnosis and treatment, detection of disease susceptibility genes, sequencing services and other fields.
Parameters

Qualification CE

Kit components

No. Product Name Spec.

S1006E Multi-type Sample DNA/RNA Extraction-Purification Kit 24T/kit

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Nucleic Acid (DNA/RNA) Extraction or Purification Kit

DNA/RNA Extraction Reagents

Brief

Nucleic Acid (DNA/RNA) Extraction or Purification Kit developed based on Sansure advanced magnetic beads technology platform, using exclusive modified super-paramagnetic nano-beads to absorb sample DNA/RNA , only needs a simple step of washing to obtain high purity nucleic acid, combined with the "DNA/RNA elution-free" technology and integrated high-efficient amplification system, to achieve DNA/RNA amplification detection with magnetic beads.

Kit components

Cat. No.	Product Description	Package	Registration
S100IE	Nucleic Acid (RNA) Extraction or Purification Kit (Magnetic beads method) Specimen types: Serum or plasma	24T/48A/48B/64T	CE NMPA
S1004E	Red Blood Cell Lysis Buffer	48T	CE NMPA
S1006E	Multi-type Sample DNA/RNA Extraction–Purification Kit (Magnetic beads method) Specimen types: serum, plasma, throat swab, genital secretion, cervical exfoliated cells	24T/48T/96T	CE NMPA
S1001E	Nucleic acid extraction (DNA/RNA) or purification kit (Magnetic beads method) Specimen types: throat swab, herpetic fluid, anal swab, feces, etc	24T/48T	CE NMPA
S10012E	Nucleic acid extraction (DNA) or purification kit (Magnetic beads method) Specimen types: Serum or plasma	48T/96T/48A/48B	CE NMPA
S10013E	Nucleic acid extraction (DNA/RNA) or purification kit (Magnetic beads method) Specimen types: Serum or plasma	24T/48T/48A/48B	CE NMPA
S10016E	Nucleic Acid Extraction–Purification Kit Specimen types: pharyngeal swabs, nasopharyngeal swabs, alveolar lavage fluid, sputum, saliva, plasma, serum, stool and anal swabs Specifications may vary depending on the extraction instruments	24T/48T/96T/24A/24B/ 48A/48B/48C/64T/96A	CE NMPA
S50016E	Nucleic Acid Extraction-Purification Kit Specimen types:pharyngeal swabs,nasopharyngeal swabs,oliveolar lavage uid sputum,saliva,plasma,serum,stool,oral swabs and exfoliated cells from females’ cervix,etc. Specifications may vary depending on the extraction instruments	48T/96T/12A/24A/24B/ 32A/32T/32S/48A/48B/ 48C/64A/64T/96A	CE NMPA
S5006E	Nucleic Acid Extraction-Purification Kit V–VI Specimen types:whole blood,serum,plasma.	48T/48A/48B/64T	CE
S5007E	Nucleic Acid Extraction-Purification Kit V–VII Specimen types:cervical swab,opharyngeal swab,nasopharyngeal swabs,anal swab,rectal and vaginal swabs.	48T/96T/48A/64T/96A	CE

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Sample release reagent
DNA/RNA Extraction Reagents

Brief
Sample release reagent developed based on the Sansure one-tube fast release technology platform. Adopting Sansure patent nucleic acid release technology, can quickly lyse pathogens at room temperature, no need heating, centrifuging or replacing tubes, the sample DNA/RNA can be extracted quickly through simple operations. Sample Release Reagent is used for the pretreatment of nucleic acids, to release the nucleic acids from specimens, then the released nucleic acids can be used for clinical in vitro diagnosis or used for the detection through equipment.
Parameters

Qualification CE

Kit components

No. Product Name Spec.

S1011E Sample Release Reagent 48T/kit

S1013E Sample Release Reagent 48T/kit

S1014E Sample Release Reagent 24T/Kit, 48T/kit

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High sensitivity

HBV 3IU/mL
HCV 10IU/mL
HIV 45IU/mL

High efficiency

576 tests/ ~5h(pooling)
45 tests / ~4.5h(single)

Complete subtypes coverage

HBV A-H
HCV 1-6
HIV-1（M/N/O）and HIV-2

Multiple results in one test

4 tests in one test
Direct discriminative positive results

Automated detection

Extraction and amplification process
Fully automated extraction and amplification

Cost and space savings

One extractor + one amplifier
Less consumable material consumption

Parameters

Items	C003E
Product Name	Nucleic Acid Test Kit for HBV, HCV, HIV (Type1+2) (Real-time PCR)
Package Specification	96 tests/kit
Amplification	Amplification Multiplex real-time PCR
Extraction	Magnetic bead method
Sample type	Plasma
Sample Volume	960μL
LoD	Individual testing: HBV 3 IU/mL; HCV 10 IU/mL; HIV 45 IU/mL Mini-pool testing: HBV 18 IU/mL; HCV 60 IU/mL; HIV 270 IU/mL
Storage and Validity	Amplification kit: −25 to −15°C, 12months; Extraction kit: 2 – 8°C, 12 months
Qualification	NMPA

Related Instruments

S3034E HCV Genotype – Hepatitis C Virus Genotype Diagnostic Kit

Brief

By applying real-time PCR technology, the Hepatitis C Virus Genotype Diagnostic Kit (PCR-Fluorescence Probing) is designed for qualitative identification of HCV genotypes (including genotypes 1b, 1, 2, 3, 4, 5 and 6) from HCV RNA positive samples. The test results can be used as an aid in the identification of HCV genotypes and determination of an appropriate therapeutic treatment indicated for the above listed gentoypes. The results can be used only for clinical reference, and cannot be used as the only evidence for adjusting therapeutic drugs. Clinical symptoms and other laboratory test results should also be considered to comprehensively determine the patients treatment.

Parameters

Product features	Parameter
Specimen Type	Serum
Extraction Platform	Magnetic beads technologies
Genotype	1(1b, 1a), 2 (2a), 3 (3a, 3b), 4 (4a), 5 (5a), 6 (6a)
Internal Control	Plasmid
PCR Instrument	Mx3000P, SLAN-96P
Sensitivity	1000 IU/mL
Spec.	12T
Qualification	CE

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S3119E HCV Ultra – Hepatitis C Virus RNA Quantitative Fluorescence Diagnostic Kit

Brief

Hepatitis C Virus RNA Quantitative Fluorescence Diagnostic Kit (PCR-Fluorescence Probing) is intended for quantitative detection of the Hepatitis C Virus RNA in human EDTA plasma specimens. The Hepatitis C Virus genotypes 1, 2, 3, 4, 5, 6, can be quantitatively detected.
Test results shall not be used as the only indicator for clinical diagnosis, and a comprehensive analysis of the condition must be conducted in combination with the patient's clinical manifestations and other laboratory tests.
The kit Must NOT be used for blood screening.
For in vitro diagnostic use only. For professional use only.

Parameters

Product features	Parameter
Specimen Type	Plasma
Extraction Platform	Advanced magnetic beads technology
Genotype	HCV 1-6 genotype
Internal Control	Lentivirus particles
PCR Instrument	SLAN-96P, ABI7500, Roche cobas 480
Sensitivity	12 IU/mL
Linear range	25—1.0E+08 IU/mL
Spec.	24T

Order Information

Cat. No.	Product Name	Spec.
S3119E-24	Hepatitis C Virus RNA Quantitative Fluorescence Diagnostic Kit (PCR-Fluorescence Probing)	24T
S10013E-48	Nucleic acid extraction (DNA) or purification kit (Magnetic beads method)	48T

Related Instruments

S3013E HBV Fast – Hepatitis B Virus DNA Quantitative Fluorescence Diagnostic Kit

Brief

Hepatitis B Viral (HBV) DNA Quantitative Fluorescence Diagnostic Kit (PCR-Fluorescence Probing) is an in vitro nucleic acid amplification test for the quantification of HBV DNA in human serum or plasma. It can be used to evaluate antiviral treatment and monitor the therapeutic effect by monitoring HBV DNA baseline levels and changes in patient blood. Test results should not be taken as the only indicator for evaluation of diseases, but to be combined with patients clinical symptoms and other laboratory tests to analyze the diseases.

Parameters

Product features	Parameter
Specimen Type	Serum or plasma
Extraction Platform	One-tube fast release
Genotype	HBV genotype A-H
Internal Control	Plasmid
Compatible Instrument	ABI7300 , Stratagene Mx3000P , Roche Light Cycler 480 , ABI7500, SLAN-96P and QuantStudio 5
Limit of Detection	30 IU/mL
Linear range	100—5.0E+09 IU/mL
Spec.	24T, 48T

Order Information

Cat. No.	Product Name	Spec.
S3013E	Hepatitis B Virus DNA Quantitative Fluorescence Diagnostic Kit (PCR-Fluorescence Probing)	24T, 48T
S1011E	Sample Release Reagent	48T

Related Instruments

S3118E HBV Ultra – Hepatitis B Virus DNA Quantitative Fluorescence Diagnostic Kit

Brief

Hepatitis B Virus DNA Quantitative Fluorescence Diagnostic Kit (PCR-Fluorescence Probing) is intended for quantitative detection of the Hepatitis B Virus DNA in human EDTA plasma specimens. The Hepatitis B Virus genotypes A, B, C, D, E, F, G, H can be quantitatively detected.
Test results shall not be used as the only indicator for clinical diagnosis, and a comprehensive analysis of the condition must be conducted in combination with the patient's clinical manifestations and other laboratory tests.
The kit Must NOT be used for blood screening.
For in vitro diagnostic use only. For professional use only.

Performance

Advanced magnetic beads technology HBV DNA detection and viral load measurement are essential for treatment decisions and patient monitoring. Sansure's HBV Ultra uses the advanced magnetic beads technology to extract HBV DNA from clinical Plasma. Our technology achieved high sensitivity and wide linear range detection to meet of clinical diagnosis and follow-up needs. Highly conservative primer probe design Sansure primers and probes target select the highly conservative S gene of HBV, which can cover A-H genotypes and avoid missed detection. High-efficient quality control system HBV Ultra uses UNG enzyme + dUTP system to remove carry-over contamination to avoid a false positive result. HBV Ultra uses Internal Control HBV Ultra uses Internal Control is the full name to whole-process the HBV extraction and amplification process to avoid false negative results.

Parameters

Product features	Parameter
Specimen Type	Plasma
Extraction Platform	Advanced magnetic beads technology
Genotype	HBV genotype A-H
Internal Control	Pseudoviruses
PCR Instrument	SLAN-96P, ABI7500, Roche cobas 480
Sensitivity	5 IU/mL
Linear range	20—2.0E+09 IU/mL
Spec.	48T

Order Information

Cat. No.	Product Name	Spec.
S3118E-48	Hepatitis B Virus DNA Quantitative Fluorescence Diagnostic Kit (PCR-Fluorescence Probing)	48T
S10012E-48	Nucleic acid extraction (DNA) or purification kit (Magnetic beads method)	48T

Product features	Parameters
Specimen Type	Oropharyngeal swab, sputum
Extraction Platform	One-tube fast release technology Advanced magnetic beads technology
Target Genes	SARS-CoV-2：ORF 1ab, N gene； influenza A：M gene； influenza B：NP gene
Internal Control	Rnase P gene
PCR Instrument	ABI7500, SLAN-96P, MA-6000, QuantGene 9600, iPonatic S-Q31A&B,S-Q36A
Sensitivity	200 copies/mL
Spec.	24T, 48T, 24-P
Qualification	CE

S3148E SC2/Flu/RSV – SARS-CoV-2, Influenza Virus and Respiratory Syncytial Virus Multiple Nucleic Acid Diagnostic Kit

Brief

The SARS-CoV-2, Influenza Virus and Respiratory Syncytial Virus Multiple Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing) is a real-time RT-PCR test intended for the qualitative Diagnostic of nucleic acid from SARS-CoV-2, Influenza Virus and Respiratory Syncytial Virus Multiple in the nasopharyngeal swabs and oropharyngeal swabs from individuals.

As the seventh coronavirus that infects humans, the SARS-CoV-2 can cause fever, fatigue, dry cough, dyspnea and other symptoms. In severe cases, it can cause acute respiratory distress syndrome, septic shock, and even death. At the same time, the SARS-CoV-2 has a strong spreading ability and has a wide range. Influenza virus (Influenza virus) can cause acute respiratory infections, with clinical manifestations of fever, headache, myalgia, fatigue, rhinitis, sore throat and cough. Influenza viruses can aggravate underlying diseases (such as heart and lung diseases) or cause secondary bacterial pneumonia or primary influenza viral pneumonia. The elderly and people with various chronic diseases or physical weakness are prone to severe complications and mortality higher after infecting influenza. Respiratory syncytial virus (RSV) belongs to the Pneumovirus genus of the Paramyxoviridae family. It mainly causes lower respiratory tract infections such as bronchiolitis and pneumonia in infants under 6 months, as well as rhinitis , Cold and other upper respiratory tract infections in older children and adults.

Parameters

Product features	Parameter
Covering pathogens	SARS-CoV-2, Influenza Virus and Respiratory Syncytial Virus
Specimen Types	Nasopharyngeal swab and oropharyngeal swab
Technical Platform	One-tube fast release technology Advanced magnetic beads technology
Internal Control	RNase P gene
Compatible Instrument	ABI 7500; MA-6000; SLAN®-96P; iPonatic S-Q31A/S-Q31B/S-Q36A
Sensitivity	500 copies/mL.
Qualification	CE

S3102E SC2 – Novel Coronavirus (2019-nCoV) Nucleic Acid Diagnostic Kit