This qualitative test detects Group A Streptococcus antigen directly from throat swab specimens.
With high accuracy and simple two-color results in just 5 minutes, it aids in effective diagnosis and responsible antibiotic use, all without needing additional equipment.
This test is US FDA-cleared, and also HSA-registered.
For clinical professional use only.
Easy-to-read two color results
96% sensitivity;
98% specificity versus culture
Results in 5 minutes
Manufactured by OSOM® (USA) under Seikisui Diagnostics.
Hangzhou AllTest
The Syphilis Rapid Test is for the qualitative detection of antibodies (IgG and IgM) to Treponema Pallidum (TP) in specimen with the use of LF Reader. It is to aid in the diagnosis of Syphilis.
Specifications
Principle: Chromatographic Immunoassay
Format: Cassette
Specimen: Whole Blood/ Serum/Plasma
Certificate: CE
Reading Time: 5 minutes
Pack Size: 25 Tests/Box
1 x Syphilis Rapid Test Cassette
1 x Dropper
1 x Buffer Solution
Product Insert
Rovers®
The Evalyn® Brush is a reliable self-sampling device used for screening for Human Papillomavirus (HPV), the leading cause of cervical cancer. It has been widely used in the Dutch Screening Program for cervical cancer prevention. The device allows women to take samples at home, overcoming barriers like time constraints, discomfort, or cultural concerns. By offering a safe, easy, and comfortable method, the Evalyn® Brush encourages more women to participate in timely screening, helping prevent cervical cancer.
Comfortable and effective: Features flexible bristle technology for maximum sample yield with minimal discomfort.
Hygienic and secure: Sterilized, individually packed, and labeled with 2D barcodes or data matrices for easy tracking.
User-friendly: Comes with full-color instructions, step-by-step graphics, and built-in features to ensure correct sampling.
Convenient and efficient: No liquid required for mailing the sample, and an RFID chip is available for fast lab processing.
Trusted and validated: Made in the Netherlands, validated with PCR-based assays, and selected by the Dutch and Danish screening programs as the top self-sampling device.
Designed by women for women: Tailored to women’s needs for ease and reliability.
Hangzhou AllTest
The HCV Rapid Test is for the qualitative detection of the presence of antibody to HCV in specimen that can be performed with the use of LF Reader. It can be used to aid in the diagnosis of Hepatitis C.
Pack size: 40-tests/box
Fast results, 10 mins
Easy visual interpretation
Simple operation, no equipment required
High accuracy
Hangzhou AllTest
hCG Pregnancy Urine Rapid Test
This test provides results for qualitative detection of hCG in urine to aid in early pregnancy detection.
Pack size: 40-tests/box
Fast results, 3 mins – 5 mins
Easy visual interpretation
Simple operation, no equipment required
High accuracy
The test approved by US-FDA, and also approved by HSA in Singapore. For clinical professional use only
Measuring the total haemoglobin concentration for anaemia in the blood
hemochroma PLUS is a handheld device that can run tests for anaemia. The hemochroma PLUS offers instant access to hemoglobin and calculated hematocrit results, empowering healthcare professionals to make real-time treatment decisions
US FDA 510(K) CLIA waived
Quick test results in 3 seconds
User-friendly graphic interface
Stores 1,000 results onboard
Cleared for patients 6 months or older
Reagent-free microcuvettes
Microcuvette shelf life of up to 2 years, even afterthe canister has been opened
Measurement range 5.0 to 25.6 g/dL
Small 15 ul sample volume
3.25″ Color LCD Display
AFIAS-6
Automated Immunoassay Analyser with the all-in-one cartridge system
AFIAS-6 is a unique integrated (sample-to-answer) system. It features 6 parallel tests of differing parameters, fast turn-around, and high sensitivity, rivalling those of the full-featured systems in commercial labs.
Automated POCT system with All-in-One cartridges
Easy to use with proprietary C-tips (for fingertip blood)
Up to 6 different parallel tests
HSA registered
T2Bacteria® Panel: It’s the first FDA-cleared and CE-marked test panel capable of identifying six common bacterial pathogens.
Time Efficiency: Delivers results in 3 to 5 hours directly from a whole blood sample.
Pathogens Detected: Includes E. faecium, S. aureus, K. pneumoniae, A. baumannii, P. aeruginosa, and E. coli.
Clinical Relevance: These bacteria are prevalent in emergency departments and are often responsible for hospital-acquired infections.
ESKAPE Pathogens: Some detected species are ESKAPE pathogens, known for their virulence and resistance to empiric antimicrobial therapy.
Impact on Patient Care: Quick identification of these pathogens is crucial for timely and targeted treatment, which can significantly improve patient outcomes.
Innovation: The T2Dx Instrument represents a breakthrough in diagnostic technology, enabling direct detection from whole blood samples.
Automation: Fully automated system with walk-away operation, minimising human intervention once the test is set up.
Efficiency: Can run multiple tests simultaneously directly from whole blood, without prior sample preparation.
Capabilities: The T2Dx Instrument provides rapid results, within 3 to 5 hours.
User-Friendly: Simple user interface with a touchscreen display. Step-by-step text and illustrative prompts for easy operation.
Versatility: The instrument can run various tests, including the HSA-registered T2Bacteria and T2Candida Panels
The OSOM Ultra Plus Flu A & B Test is an in vitro rapid qualitative test that detects influenza type A and type B nucleoprotein antigens directly from nasal swab and nasopharyngeal swab specimens obtained from patients with signs and symptoms of respiratory infection.
Meets the Influenza reclassification requirements for rapid antigen tests *Refer to the Package Insert for additional performance claims.
Simple CLIA-waived procedure with pre-measured extraction buffer for swab samples
Accurate, differentiated interpretation of results in 10 minutes to test and treat patients in one office visit
QC Inside®: 2 Additional test sticks for external QC