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ABO/RHD ANTIGEN RAPID TEST (SOLID-PHASE METHOD). - DIGEMID Registration DMDIV5934E

Access comprehensive regulatory information for ABO/RHD ANTIGEN RAPID TEST (SOLID-PHASE METHOD). in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV5934E and manufactured by AIKANG DIAGNOSTICS Co., Ltd.. The device was registered on December 23, 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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DMDIV5934E
ABO/RHD ANTIGEN RAPID TEST (SOLID-PHASE METHOD).
DIGEMID ID: DMDIV5934E
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Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV5934E
Registration Date
December 23, 2024
Expiration Date
December 23, 2029
Creation Date
March 10, 2025
Authorized Representative