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Peru DIGEMID registration DMDIV5586E

04Z23 TBI (04W17 GFAP REAGENT KIT, 04W19 UCH-L1 REAGENT KIT).

Peru flagPeru·IN VITRO MEDICAL DEVICE·ABBOTT IRELAND DIAGNOSTICS DIVISION·Registered May 31, 2024
Device classification
Product Type
IN VITRO MEDICAL DEVICE
Registration information
Analysis ID
DMDIV5586E
Registration Date
May 31, 2024
Expiration Date
May 31, 2029
Creation Date
March 10, 2025
Manufacturer
Name
ABBOTT IRELAND DIAGNOSTICS DIVISION
Authorized Representative
Name
ABBOTT LABORATORIES S.A.
About this record

Access comprehensive regulatory information for 04Z23 TBI (04W17 GFAP REAGENT KIT, 04W19 UCH-L1 REAGENT KIT). in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV5586E and manufactured by ABBOTT IRELAND DIAGNOSTICS DIVISION. The device was registered on May 31, 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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