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The ACCULYNE Nitrile Examination gloves are high performing 0.07 mm thickness powder-free blue coloured ambidextrous gloves that are intended for use in medical field to: protect patient and user from cross contamination, conducting medical examinations, diagnostic and therapeutic procedures and for handling medical contaminated material. This examination glove product conforms under International, American and European standards specific to: FDA device list code LZA, ASTM D6319-10, ASTM D6978-05, EN ISO 16523, EN 21420, EN374 and EN455.

Materials Pure - Nitrile
Type - Latex-Free, Odour-Free and Powder-Free
Surface Treatments - Polymer Coated
Colour - Light Blue
Characteristics - Acrylonitrile Butadiene Rubber
Sterilization = Non Sterlie Ambidextrous Beaded Cuf
Use - Single use only

Key Features
Latex-Free 100% Nitrile
Anti-static, surface resistance 109 ohms
Powder Free
Beaded Cuff
Fully textured finger tips
3X Puncture Resistance of vinyl or latex gloves
Pack: 100 gloves/dispenser boxes
Industrial Applications
Assembly
Inspection
Medical
Dental
Surgical
Laboratory/ EMS
Pharmaceutical manufacturing
Painting and fishing
Food processing/packing
Cleaning

We, IREC GROUP and IREC GLOVE INDUSTRY (THAILAND) CO., LTD. hereby state that we own and hold the commercial rights of the ACCULYNE�® GLOVES brand of nitrile gloves. and can provide all necessary legal certifications/documents for export-import, sales and warranty. It is recognized and used by countries/states/countries around the world.

Self-test received notified body approved CE marking on April 1, 2021
A home test for the rapid qualitative detection of SARS-CoV-2 virus antigen in anterior nasal swabs within 7 days of symptom onset

Performance Characteristics
Sample type: nasal swab
Time to result: 15-20 min
Sensitivity: 96.77%
Specificity: 99.20%
Accuracy: 98.72%
Layperson study statistics:
o 99.10% of non-professionals carried out the test without requiring assistance
o 97.87% of different types of results were interpreted correctly

Kit Components:
1 Rapid SARS-CoV-2 Antigen Test Card (sealed foil pouch)
1 sterilized swab
1 extraction tube
1 sample extraction buffer
IFU
1 tube stand

This kit is only used for the in vitro qualitative detection of 2019-nCoV antigen from
human nasopharyngeal swab, nasal swab or oropharyngeal swab specimens.
This kit is suitable for the auxiliary diagnosis of COVID-19, the results are for clinical
reference only and cannot be used as the sole basis for diagnosis and exclusion
decision. The clinical diagnosis and treatment of patients should be considered in
combination with their symptoms/signs, medical history, other laboratory tests and
treatment responses.
Positive test result needs to be further confirmed, negative result does not preclude
2019-nCoV infection.
This kit is intended for use by qualified and trained clinical laboratory personnel
specifically instructed and trained in the techniques of in vitro diagnostic procedures.
TEST PRINCIPLE
The kit is immunochromatographic and uses double-antibody sandwich method to
detect 2019-nCoV N protein antigen. During detection, the treated specimens are
loaded into the sample wells of the test card. When the concentration of 2019-nCoV
antigen in specimen is higher than the minimum detection limit, the viral antigen will
form complexes with labeled antibodies first. Under chromatography, the complexes
move forward along the nitrocellulose membrane till captured by pre-coated
monoclonal antibody of 2019-nCoV in detection zone on nitrocellulose film (T) to
form a pink/purple reaction line on the detection zone, at this point the result is
positive; conversely, if there is no viral antigen or the concentration of antigen in
specimen is below the minimum detection limit, no pink/purple reaction line appears
in the detection zone, at this point the result is negative. Regardless of whether the
sample contains viral antigens or not, a pink/purple reaction line will appear in the
quality control zone (C), the pink/purple reaction line that appears in the quality
control zone (C) is the criterion for determining if the chromatography process is
normal.