E8 MedTech is a National Minority Supplier of OEM PPE and Commodities. E8 MedTech is a revolutionary PPE distributor of Medical Devices and Supplies with innovative solutions for today's global market. E8 MedTech provides medical equipment and commodity to government agencies, testing centers, hospitals, professional sports organizations, and private entities.

E8 MedTech is a privately-owned company that distributes and markets PPE products for companies like Celltrion, Healgen, Access Bio, and Best-Rx. The pharmaceutical industry is ever-changing. Understanding and countering these challenges with new and improved products is our goal. Our strategy is understanding technology and science combined with knowledge of the needs of our consumers.

PPE KIT

CUSTOM KIT INCLUDES

3x 3 Ply Disposable Facial Mask

1x 60ML Hand Sanitizer (62% Alcohol)

3x Hand Wipes (70% Alcohol)

The BEST-Rx 3Ply facial masks come with a pliable nosepiece for a more comfortable fit. This PPE KIT is an example of a custom order KIT.

Please CONTACT US with PPE product inquires

Celltrion DiaTrust™ COVID-19 Ag Rapid Test (POC)

Celltrion DiaTrust™ COVID-19 Ag Rapid Test is a rapid test based on lateral flow immunoassay intended for the qualitative detection of nucleocapsid and receptor binding domains (RBDs) from the SARS-CoV-2 spike proteins in human nasopharyngeal swab specimen.

Product
Specification:

Sample Type

Mid-Turbinate Nasal Swab (NS)

Sample-to-answer time

15 mins

FDA Status

FOR USE UNDER THE EMERGENCY USE AUTHORIZATION (EUA) ONLY

Authorized Laboratories

Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation (Waived, Moderate or High)

Intended Use:

Celltrion DiaTrust™ COVID-19 Ag Rapid Test is a rapid test based on lateral flow immunoassay intended for the qualitative detection of nucleocapsid and receptor-binding domains (RBDs) from the SARS-CoV-2 spike proteins in human nasopharyngeal swab specimen. Results are for the identification of SARS-CoV-2 nucleocapsid and RBD protein antigen.

This product has not been FDA cleared or approved, but has been authorized by FDA under a EUA for use by authorized laboratories;
This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens and,
The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for the detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. 360bbb-3(b)(1) unless the declaration is terminated or authorization is revoked sooner