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HIGH-RISK HUMAN PAPILLOMAVIRUS DNA (GENOTYPE) DIAGNOSTIC KIT (PCR-FLUORESCENCE PROBING). - DIGEMID Registration DMDIV4222E

Access comprehensive regulatory information for HIGH-RISK HUMAN PAPILLOMAVIRUS DNA (GENOTYPE) DIAGNOSTIC KIT (PCR-FLUORESCENCE PROBING). in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV4222E and manufactured by SANSURE BIOTECH INC.. The device was registered on December 07, 2021.

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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DMDIV4222E
HIGH-RISK HUMAN PAPILLOMAVIRUS DNA (GENOTYPE) DIAGNOSTIC KIT (PCR-FLUORESCENCE PROBING).
DIGEMID ID: DMDIV4222E
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Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV4222E
Registration Date
December 07, 2021
Expiration Date
December 07, 2026
Creation Date
March 10, 2025
Manufacturer
Authorized Representative