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AFIAS COVID-19 AG, MARCH: AFIAS - DIGEMID Registration DMDIV3540E

Access comprehensive regulatory information for AFIAS COVID-19 AG, MARCH: AFIAS in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV3540E and manufactured by BODITECH WITH INC.. The device was registered on September 14, 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.

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DIGEMID Official Data
DMDIV3540E
AFIAS COVID-19 AG, MARCH: AFIAS
DIGEMID ID: DMDIV3540E
Local name: AFIAS COVID-19 AG, MARCA: AFIAS
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Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV3540E
Registration Date
September 14, 2020
Expiration Date
September 14, 2025
Creation Date
March 10, 2025
Manufacturer
Authorized Representative