Peru DIGEMID registration DMDIV5175E

ALLPLEX™ RESPIRATORY PANEL 1, ALLPLEX™ RESPIRATORY PANEL 2, ALLPLEX™ RESPIRATORY PANEL 3, ALLPLEX™ GI-BACTERIA (I) ASSAY, ALLPLEX™ GI-BACTERIA (II) ASSAY.

Peru·IN VITRO MEDICAL DEVICE·SEEGENE INC.·Registered October 25, 2023

Device classification

Product Type: IN VITRO MEDICAL DEVICE

Registration information

Analysis ID: DMDIV5175E
Registration Date: October 25, 2023
Expiration Date: October 25, 2028
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 ALLPLEX™ RESPIRATORY PANEL 1, ALLPLEX™ RESPIRATORY PANEL 2, ALLPLEX™ RESPIRATORY PANEL 3, ALLPLEX™ GI-BACTERIA (I) ASSAY, ALLPLEX™ GI-BACTERIA (II) ASSAY. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV5175E and manufactured by SEEGENE INC.. The device was registered on October 25, 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.