Peru DIGEMID registration DMDIV5022E

DENGUE IgG/IgM TEST; DENGUE NS1 AG TEST; DENGUE IgG/IgM + NS1 COMBO TEST, MARCA: CORE TESTS®

Peru·IN VITRO MEDICAL DEVICE·CORE TECHNOLOGY CO., LTD.·Registered July 05, 2023

Device classification

Product Type: IN VITRO MEDICAL DEVICE

Registration information

Analysis ID: DMDIV5022E
Registration Date: July 05, 2023
Expiration Date: July 05, 2028
Creation Date: March 10, 2025

Manufacturer

Name: CORE TECHNOLOGY CO., LTD.

Authorized Representative

Name: MULTIMEDICAL SUPPLIES S.A.C.

About this record

Access comprehensive regulatory information for DENGUE IgG/IgM TEST; DENGUE NS1 AG TEST; DENGUE IgG/IgM + NS1 COMBO TEST, MARCA: CORE TESTS® in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV5022E and manufactured by CORE TECHNOLOGY CO., LTD.. The device was registered on July 05, 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.