VIDAS® TBI (GFAP, UCH-L1). - DIGEMID Registration DMDIV5963E
Access comprehensive regulatory information for VIDAS® TBI (GFAP, UCH-L1). in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV5963E and manufactured by BIOMERIEUX S.A.. The device was registered on January 22, 2025.
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
DMDIV5963E
VIDAS® TBI (GFAP, UCH-L1).
DIGEMID ID: DMDIV5963E
Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV5963E
Registration Date
January 22, 2025
Expiration Date
January 22, 2030
Creation Date
February 17, 2025
Manufacturer
Name
BIOMERIEUX S.A.Authorized Representative

