RevMed
Home/Zika ELITe MGB® - EUA

Elitechgroup Mdx LLC M800552 Zika ELITe MGB® - EUA

Company Name
Elitechgroup Mdx LLC
Catalog Number
M800552

Description

The United States (US) Food and Drug Administration (FDA) has issued an Emergency UseAuthorization (EUA) to authorize the use of the Zika ELITe MGB® Kit U.S. for the in vitroqualitative detection of Zika virus with specified instruments. This assay tests for Zika virusRNA in human serum and EDTA plasma.
Have questions or need more information? Contact Us
RevMed is an independent marketplace for reselling medical devices and equipment. We are not affiliated with or endorsed by manufacturers, and all trademarks and brand names belong to their respective owners. Product images and descriptions are for reference only, and RevMed does not provide medical advice, training, or support.
Find Savings Automatically!
Your trusted browsing companion

Additional Details

Device Identifier
03661540950018
Is RX
Yes
Is Over the Counter
No
Requires Sterilization
No
Is Sterile
No
Is Single Use
No

Barcode Mapping

Unit of MeasurementEachesGTIN
Each103661540950018