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HI-PCR HUMAN PAPILLOMA VIRUS (HPV) GENOTYPING (16,18 & 45 MULTIPLEX) PROBE PCR KIT. - DIGEMID Registration DMDIV5321E

Access comprehensive regulatory information for HI-PCR HUMAN PAPILLOMA VIRUS (HPV) GENOTYPING (16,18 & 45 MULTIPLEX) PROBE PCR KIT. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV5321E and manufactured by HIMEDIA LABORATORIES PVT. LTD. The device was registered on January 12, 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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DMDIV5321E
HI-PCR HUMAN PAPILLOMA VIRUS (HPV) GENOTYPING (16,18 & 45 MULTIPLEX) PROBE PCR KIT.
DIGEMID ID: DMDIV5321E
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Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV5321E
Registration Date
January 12, 2024
Expiration Date
January 12, 2029
Creation Date
March 10, 2025