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Peru DIGEMID registration DMDIV5925E

ISE INTERNAL STANDARD GEN.2.

Peru flagPeru·IN VITRO MEDICAL DEVICE·ROCHE DIAGNOSTICS GMBH·Registered December 19, 2024
Device classification
Product Type
IN VITRO MEDICAL DEVICE
Registration information
Analysis ID
DMDIV5925E
Registration Date
December 19, 2024
Expiration Date
December 19, 2029
Creation Date
February 17, 2025
Manufacturer
Name
ROCHE DIAGNOSTICS GMBH
Authorized Representative
Name
ROCHE PRODUCTS Q.F.S.A.
About this record

Access comprehensive regulatory information for ISE INTERNAL STANDARD GEN.2. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV5925E and manufactured by ROCHE DIAGNOSTICS GMBH. The device was registered on December 19, 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.

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