DXH 500 SERIES LYSE. - DIGEMID Registration DMDIV4340E
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.
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DIGEMID Official Data
DMDIV4340E
DXH 500 SERIES LYSE.
DIGEMID ID: DMDIV4340E
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
Authorized Representative

