kPCR PLX®, according to detail. - DIGEMID Registration DMDIV2357E
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 DMDIV2357E and manufactured by ALTONA DIAGNOSTICS GmbH. The device was registered on July 05, 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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DMDIV2357E
kPCR PLX®, according to detail.
DIGEMID ID: DMDIV2357E
Local name: kPCR PLX®, según detalle.
Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV2357E
Registration Date
July 05, 2017
Expiration Date
July 05, 2022
Creation Date
March 10, 2025
Manufacturer
Authorized Representative
Name
SIEMENS S.A.C.
