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VITEK®MS MOLD KIT, MARCA: VITEK - DIGEMID Registration DMDIV5229E

Access comprehensive regulatory information for VITEK®MS MOLD KIT, MARCA: VITEK in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV5229E and manufactured by BIOMERIEUX S.A.. The device was registered on November 21, 2023.

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
DMDIV5229E
VITEK®MS MOLD KIT, MARCA: VITEK
DIGEMID ID: DMDIV5229E
Local name: VITEK®MS MOULD KIT, MARCA: VITEK
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Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV5229E
Registration Date
November 21, 2023
Expiration Date
November 21, 2028
Creation Date
March 10, 2025
Manufacturer
Authorized Representative