Peru DIGEMID registration DMDIV4865E

HUMAN PAPILLOMAVIRUS DNA (23 GENOTYPES) DIAGNOSTIC KIT (PCR-FLUORESCENCE PROBING), CHLAMYDIA TRACHOMATIS / UREAPLASMA UREALYTICUM / NEISSERIA GONORRHOEAE DNA DIAGNOSTIC KIT (PCR-FLUORESCENCE PROBING), MYCOBACTERIUM TUBERCULOSIS DNA FLUORESCENCE DIAGN

Peru·IN VITRO MEDICAL DEVICE·SANSURE BIOTECH INC.·Registered March 13, 2023

Device classification

Product Type: IN VITRO MEDICAL DEVICE

Registration information

Analysis ID: DMDIV4865E
Registration Date: March 13, 2023
Expiration Date: March 13, 2028
Creation Date: February 17, 2025

Manufacturer

Name: SANSURE BIOTECH INC.

Authorized Representative

Name: QUALITY INSTITUTE ERROCH S.A.C

About this record

Access comprehensive regulatory information for HUMAN PAPILLOMAVIRUS DNA (23 GENOTYPES) DIAGNOSTIC KIT (PCR-FLUORESCENCE PROBING), CHLAMYDIA TRACHOMATIS / UREAPLASMA UREALYTICUM / NEISSERIA GONORRHOEAE DNA DIAGNOSTIC KIT (PCR-FLUORESCENCE PROBING), MYCOBACTERIUM TUBERCULOSIS DNA FLUORESCENCE DIAGN in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV4865E and manufactured by SANSURE BIOTECH INC.. The device was registered on March 13, 2023.

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.