15 HIGH-RISK HUMAN PAPILLOMAVIRUS DNA DIAGNOSTIC KIT (PCR-FLUORESCENCE PROBING). - DIGEMID Registration DMDIV4255E
Access comprehensive regulatory information for 15 HIGH-RISK HUMAN PAPILLOMAVIRUS DNA 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 DMDIV4255E and manufactured by SANSURE BIOTECH INC.. The device was registered on January 04, 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
DMDIV4255E
15 HIGH-RISK HUMAN PAPILLOMAVIRUS DNA DIAGNOSTIC KIT (PCR-FLUORESCENCE PROBING).
DIGEMID ID: DMDIV4255E
Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV4255E
Registration Date
January 04, 2022
Expiration Date
January 04, 2027
Creation Date
March 10, 2025
Manufacturer
Authorized Representative

