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U.S. BASED PRODUCTS
WeScan - COVID-19 Entry Access Management System
WeScan - COVID-19 Entry Access Management System
WeScan - COVID-19 Entry Access Management System
By preventing the spread of viruses, you can maintain a safe and healthy workplace while providing peace-of-mind to anxious staff, patients, students, visitors and the general public.
3 Layer Surgical Face Mask
WeScan - COVID-19 Entry Access Management System
WeScan - COVID-19 Entry Access Management System
Our mask is a 3 ply unit using the standard melt blown middle layer rated at 28 CFM. This test is used for FDA 510(k) submissions for surgical masks; is required by ASTM F2100 and EN 14683; and complies with ASTM F2101 and EN14683.
Washable & Reusable Safety Mask
WeScan - COVID-19 Entry Access Management System
Washable & Reusable Safety Mask
Our 3-Ply barrier masks are made in the U.S. and utilize our air and water filtration fabric, a non-woven water repellent material and a comfortable jersey barrier . The masks have been tested through an infectious disease regimen; subjected to wash at 170 degrees; and passed with high reviews.
Non-U.S.-Based Products
FDA & CE APPROVED
For bulk quantities please contact us at PPEnow@transcend-inc.net
Medical Gowns
USA Standard: FDA OEA, General Surgery
EU Standard: EN 146605:2005 + A1:2009, ISO 13982-2:2004
•Medical Grade
•Protection against solid chemicals
•Protection against airborne particle
NB: Printing on masks/packages per standards (CE and FDA)
Medical Examination Gloves
USA Standard: FDA LZA, 880.6250
CE Standard: EN420:2003+A1:2009
ISO: ISO: 9001:2015, EN ISO 374-1:2006 ; EN ISO 374-4:2013; EN ISO 374-5:2016
•Premium quality, strength and durability, Nitrile/vinyl is resistant to tears, cuts, punctures, abrasives, chemicals
•Powder-free, latex-free, non-allergenic and non-irritating. The ideal solution for individuals sensitive to natural rubber latex and donning powder.
•NB: Printing on packages according to standards (CE)
IGG/IGM Test Kits
FDA EUA APPROVED
•Qualitative detection of the presence of IgM & IgG antibody to COVID-19 in Human serum, plasma and whole blood
•Results available in 10 minutes
•Component: Cassette, Sample Diluent, Pipette and Test Card
PCT Test Kits
FDA EUA APPROVED
•Real-time RT-PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2
•Results available in 1hour
•750 samples of clinical trials were completed in 3 clinical units.
•Compared with the same reagents approved for marketing, positive coincidence rate was 95.93%, negative coincidence rate was 94.07%, and the total coincidence rate was 94.80%.
For bulk quantities please contact us at PPEnow@transcend-inc.net