SARS - COV 2 ANTIBODY TEST (LATERAL FLOW METHOD) - DIGEMID Registration DMDIV3371E

Access comprehensive regulatory information for SARS - COV 2 ANTIBODY TEST (LATERAL FLOW METHOD) in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV3371E and manufactured by GUANGZHOU WONDFO BIOTECH CO. LTD.. The device was registered on March 18, 2020.

This page provides complete registration details including product type (IN VITRO MEDICAL DEVICE), manufacturer information, authorized representative details, and regulatory compliance data from the official Peru DIGEMID medical device database. Pure Global AI offers free access to Peru's complete medical device registry.