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Peru DIGEMID registration DMDIV2238E

KPCR PLX®, according to detail.

Local name: KPCR PLX®, según detalle.
Peru flagPeru·IN VITRO MEDICAL DEVICE·ALTONA DIAGNOSTICS GmbH·Registered March 03, 2017
Device classification
Product Type
IN VITRO MEDICAL DEVICE
Registration information
Analysis ID
DMDIV2238E
Registration Date
March 03, 2017
Expiration Date
March 03, 2022
Creation Date
February 23, 2023
Manufacturer
Name
ALTONA DIAGNOSTICS GmbH
Authorized Representative
Name
SIEMENS HEALTHCARE S.A.C.
About this record

Access comprehensive regulatory information for KPCR PLX®, according to detail. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV2238E and manufactured by ALTONA DIAGNOSTICS GmbH. The device was registered on March 03, 2017.

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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