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VIASURE HIGH-RISK HUMAN PAPILLOMA VIRUS REAL TIME PCR DETECTION KIT; VIASURE LEISHMANIA REAL TIME PCR DETECTION KIT. - DIGEMID Registration DMDIV4257E

Access comprehensive regulatory information for VIASURE HIGH-RISK HUMAN PAPILLOMA VIRUS REAL TIME PCR DETECTION KIT; VIASURE LEISHMANIA REAL TIME PCR DETECTION KIT. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV4257E and manufactured by CERTEST BIOTEC, S.L.. The device was registered on January 05, 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
DMDIV4257E
VIASURE HIGH-RISK HUMAN PAPILLOMA VIRUS REAL TIME PCR DETECTION KIT; VIASURE LEISHMANIA REAL TIME PCR DETECTION KIT.
DIGEMID ID: DMDIV4257E
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Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV4257E
Registration Date
January 05, 2022
Expiration Date
January 05, 2027
Creation Date
February 17, 2025
Manufacturer
Authorized Representative