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SARS-COV-2 MULTIPLEX NUCLEIC ACID DIAGNOSTIC KIT (PCR-FLUORESCENCE PROBING), SARS-COV-2AND INFLUENZA A/B VIRUS MULTIPLEX NUCLEIC ACID DIAGNOSTIC KIT (PCR-FLUORESCENCE PROBING). - DIGEMID Registration DMDIV4361E

Access comprehensive regulatory information for SARS-COV-2 MULTIPLEX NUCLEIC ACID DIAGNOSTIC KIT (PCR-FLUORESCENCE PROBING), SARS-COV-2AND INFLUENZA A/B VIRUS MULTIPLEX NUCLEIC ACID 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 DMDIV4361E and manufactured by SANSURE BIOTECH INC.. The device was registered on March 10, 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
DMDIV4361E
SARS-COV-2 MULTIPLEX NUCLEIC ACID DIAGNOSTIC KIT (PCR-FLUORESCENCE PROBING), SARS-COV-2AND INFLUENZA A/B VIRUS MULTIPLEX NUCLEIC ACID DIAGNOSTIC KIT (PCR-FLUORESCENCE PROBING).
DIGEMID ID: DMDIV4361E
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DJ Fang

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Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV4361E
Registration Date
March 10, 2022
Expiration Date
March 10, 2027
Creation Date
March 10, 2025
Manufacturer
Authorized Representative