Peru DIGEMID registration DMDIV4340E

DXH 500 SERIES LYSE.

Peru·IN VITRO MEDICAL DEVICE·BECKMAN COULTER IRELAND Inc.·Registered February 24, 2022

Device classification

Product Type: IN VITRO MEDICAL DEVICE

Registration information

Analysis ID: DMDIV4340E
Registration Date: February 24, 2022
Expiration Date: February 24, 2027
Creation Date: March 10, 2025

Manufacturer

Name: BECKMAN COULTER IRELAND Inc.

Authorized Representative

Name: DIAGNOSTICA PERUANA S.A.C.

About this record

Access comprehensive regulatory information for DXH 500 SERIES LYSE. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV4340E and manufactured by BECKMAN COULTER IRELAND Inc.. The device was registered on February 24, 2022.

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.