Peru DIGEMID registration DMDIV5321E

HI-PCR HUMAN PAPILLOMA VIRUS (HPV) GENOTYPING (16,18 & 45 MULTIPLEX) PROBE PCR KIT.

Peru·IN VITRO MEDICAL DEVICE·HIMEDIA LABORATORIES PVT. LTD·Registered January 12, 2024

Device classification

Product Type: IN VITRO MEDICAL DEVICE

Registration information

Analysis ID: DMDIV5321E
Registration Date: January 12, 2024
Expiration Date: January 12, 2029
Creation Date: March 10, 2025

Manufacturer

Name: HIMEDIA LABORATORIES PVT. LTD

Authorized Representative

Name: DROGUERIA DISTRIBUIDORA CENTA PHARMA S.A.C.

About this record

Access comprehensive regulatory information for HI-PCR HUMAN PAPILLOMA VIRUS (HPV) GENOTYPING (16,18 & 45 MULTIPLEX) PROBE PCR KIT. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV5321E and manufactured by HIMEDIA LABORATORIES PVT. LTD. The device was registered on January 12, 2024.

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.