Peru DIGEMID registration DMDIV4392E
HCV HEPATITIS C VIRUS RAPID TEST DEVICE (WHOLE BLOOD/SERUM/PLASMA).
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
About this record
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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