Peru DIGEMID registration DMDIV5434E

MEDONIC™ M-SERIES DILUENT, MEDONIC™ M-SERIES LYSE.

Peru·IN VITRO MEDICAL DEVICE·CLINICAL DIAGNOSTIC SOLUTIONS, INC·Registered April 03, 2024

Device classification

Product Type: IN VITRO MEDICAL DEVICE

Registration information

Analysis ID: DMDIV5434E
Registration Date: April 03, 2024
Expiration Date: April 03, 2029
Creation Date: March 10, 2025

Manufacturer

Name: CLINICAL DIAGNOSTIC SOLUTIONS, INC

Authorized Representative

Name: NIPRO MEDICAL CORPORATION PERU BRANCH

About this record

Access comprehensive regulatory information for MEDONIC™ M-SERIES DILUENT, MEDONIC™ M-SERIES LYSE. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV5434E and manufactured by CLINICAL DIAGNOSTIC SOLUTIONS, INC. The device was registered on April 03, 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.