Peru DIGEMID registration DMDIV3803E
ASO LATEX (SLIDE AGGLUTINATION METHOD), CRP LATEX (SLIDE AGGLUTINATION METHOD), RF LATEX (SLIDE AGGLUTINATION METHOD).
Peru·IN VITRO MEDICAL DEVICE·BEACON DIAGNOSTICS PVT. LTD.·Registered March 02, 2021Device classification
- Product Type
- IN VITRO MEDICAL DEVICE
Registration information
- Analysis ID
- DMDIV3803E
- Registration Date
- March 02, 2021
- Expiration Date
- March 02, 2026
- Creation Date
- March 10, 2025
Manufacturer
Authorized Representative
- Name
- JAMPAR S.A.C.
About this record
Access comprehensive regulatory information for ASO LATEX (SLIDE AGGLUTINATION METHOD), CRP LATEX (SLIDE AGGLUTINATION METHOD), RF LATEX (SLIDE AGGLUTINATION METHOD). in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV3803E and manufactured by BEACON DIAGNOSTICS PVT. LTD.. The device was registered on March 02, 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.
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