Peru DIGEMID registration DMDIV5425E

ANYPLEX™ II MTB/MDR DETECTION, ANYPLEX™ II MTB/XDR DETECTION.

Peru·IN VITRO MEDICAL DEVICE·SEEGENE INC.·Registered March 25, 2024

Device classification

Product Type: IN VITRO MEDICAL DEVICE

Registration information

Analysis ID: DMDIV5425E
Registration Date: March 25, 2024
Expiration Date: March 25, 2029
Creation Date: March 10, 2025

Manufacturer

Name: SEEGENE INC.

Authorized Representative

Name: GEN LAB DEL PERU S.A.C.

About this record

Access comprehensive regulatory information for ANYPLEX™ II MTB/MDR DETECTION, ANYPLEX™ II MTB/XDR DETECTION. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV5425E and manufactured by SEEGENE INC.. The device was registered on March 25, 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.