HCV HEPATITIS C VIRUS RAPID TEST DEVICE (WHOLE BLOOD/SERUM/PLASMA). - DIGEMID Registration DMDIV4392E
Access comprehensive regulatory information for HCV HEPATITIS C VIRUS RAPID TEST DEVICE (WHOLE BLOOD/SERUM/PLASMA). in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV4392E and manufactured by ABON BIOPHARM (HANGZHOU) Co., Ltd.. The device was registered on March 29, 2022.
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
DMDIV4392E
HCV HEPATITIS C VIRUS RAPID TEST DEVICE (WHOLE BLOOD/SERUM/PLASMA).
DIGEMID ID: DMDIV4392E
Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV4392E
Registration Date
March 29, 2022
Expiration Date
March 29, 2027
Creation Date
March 10, 2025
Manufacturer
Authorized Representative

