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Peru DIGEMID registration DMDIV3095E

FTD HPV HIGH RISK.

Peru flagPeru·IN VITRO MEDICAL DEVICE·FTD HPV HIGH RISK.·Registered June 05, 2019
Device classification
Product Type
IN VITRO MEDICAL DEVICE
Registration information
Analysis ID
DMDIV3095E
Registration Date
June 05, 2019
Expiration Date
June 05, 2024
Creation Date
February 06, 2024
Manufacturer
Name
FTD HPV HIGH RISK.
Authorized Representative
Name
SIEMENS HEALTHCARE S.A.C.
About this record

Access comprehensive regulatory information for FTD HPV HIGH RISK. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV3095E and manufactured by FTD HPV HIGH RISK.. The device was registered on June 05, 2019.

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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