Peru DIGEMID registration DMDIV5586E

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

Name: 04Z23 TBI (04W17 GFAP REAGENT KIT, 04W19 UCH-L1 REAGENT KIT). — DIGEMID registration DMDIV5586E
Creator: ABBOTT IRELAND DIAGNOSTICS DIVISION
Keywords: 04Z23 TBI (04W17 GFAP REAGENT KIT, 04W19 UCH-L1 REAGENT KIT)., 04Z23 TBI (04W17 GFAP REAGENT KIT, 04W19 UCH-L1 REAGENT KIT)., DMDIV5586E, IN VITRO MEDICAL DEVICE, ABBOTT IRELAND DIAGNOSTICS DIVISION, DIGEMID registration

PeruIN VITRO MEDICAL DEVICEABBOTT IRELAND DIAGNOSTICS DIVISIONRegistered May 31, 2024

VerifiedDIGEMID · official registry

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.