SARS-COV-2 IgM/IgG RAPID TEST (COVID-19 IgM/IgG RAPID TEST), MARCA: VIVADIAG™ - DIGEMID Registration DMDIV3853E
Access comprehensive regulatory information for SARS-COV-2 IgM/IgG RAPID TEST (COVID-19 IgM/IgG RAPID TEST), MARCA: VIVADIAG™ in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV3853E and manufactured by VIVACHEK BIOTECH (HANGZHOU) Co., Ltd.. The device was registered on April 09, 2021.
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.
Free Database
Powered by Pure Global AI
DIGEMID Official Data
DMDIV3853E
SARS-COV-2 IgM/IgG RAPID TEST (COVID-19 IgM/IgG RAPID TEST), MARCA: VIVADIAG™
DIGEMID ID: DMDIV3853E
Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV3853E
Registration Date
April 09, 2021
Expiration Date
April 09, 2026
Creation Date
March 10, 2025
Manufacturer
Authorized Representative

