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Peru DIGEMID registration DMDIV3249E

QUANTIA FERRITIN; QUANTIA IgE; QUANTIA RF; QUANTIA A1-ANTITRYPSIN; QUANTIA A-1-AGP; QUANTIA LP(A).

Peru flagPeru·IN VITRO MEDICAL DEVICE·BIOKIT S.A.·Registered October 30, 2019
Device classification
Product Type
IN VITRO MEDICAL DEVICE
Registration information
Analysis ID
DMDIV3249E
Registration Date
October 30, 2019
Expiration Date
October 30, 2029
Creation Date
March 10, 2025
Manufacturer
Name
BIOKIT S.A.
Authorized Representative
Name
ABBOTT LABORATORIES S.A.
About this record

Access comprehensive regulatory information for QUANTIA FERRITIN; QUANTIA IgE; QUANTIA RF; QUANTIA A1-ANTITRYPSIN; QUANTIA A-1-AGP; QUANTIA LP(A). in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV3249E and manufactured by BIOKIT S.A.. The device was registered on October 30, 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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