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HBSAG HEPATITIS B SURFACE ANTIGEN RAPID TEST DEVICE (WHOLE BLOOD-SERUM-PLASMA). - DIGEMID Registration DMDIV5953E

Access comprehensive regulatory information for HBSAG HEPATITIS B SURFACE ANTIGEN 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 DMDIV5953E and manufactured by ABON BIOPHARM (HANGZHOU) Co., Ltd.. The device was registered on January 13, 2025.

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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DMDIV5953E
HBSAG HEPATITIS B SURFACE ANTIGEN RAPID TEST DEVICE (WHOLE BLOOD-SERUM-PLASMA).
DIGEMID ID: DMDIV5953E
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Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV5953E
Registration Date
January 13, 2025
Expiration Date
January 13, 2030
Creation Date
March 10, 2025
Authorized Representative