Peru DIGEMID registration DMDIV5699E
FERRITIN TURBITEST AA.
Device classification
- Product Type
- IN VITRO MEDICAL DEVICE
Registration information
- Analysis ID
- DMDIV5699E
- Registration Date
- August 19, 2024
- Expiration Date
- August 19, 2029
- Creation Date
- March 10, 2025
Manufacturer
Authorized Representative
- Name
- LABIN PERU S.A.
About this record
Access comprehensive regulatory information for FERRITIN TURBITEST AA. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV5699E and manufactured by WIENER LABORATORIES S.A.I.C.. The device was registered on August 19, 2024.
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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