DIBU - ARCSA Registration fa51e872f97de3321f2dc2427bcf2050
Access comprehensive regulatory information for DIBU in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID fa51e872f97de3321f2dc2427bcf2050 and manufactured by ROCHE DIAGNOSTICS GMBH. The device was registered on September 03, 2023.
This page provides complete registration details including product type (In Vitro Diagnostic), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.
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ARCSA Official Data
III
fa51e872f97de3321f2dc2427bcf2050
DIBU
ARCSA ID: fa51e872f97de3321f2dc2427bcf2050
Device Classification
Risk Class
III
Product Type
In Vitro Diagnostic
Brand Name
COBAS
Commercial Name
17-408 IVD Reagents/Kits, Immunoassay, Toxicology
Registration Information
Analysis ID
fa51e872f97de3321f2dc2427bcf2050
Registration Date
September 03, 2023
Expiration Date
September 03, 2028
Product Use
IN VITRO DETERMINATION OF DIBUCAINE NUMBER FOR USE WITH THE CHOLINESTERASE IN VITRO TEST.
Manufacturer
Product Owner
Name
ROCHE DIAGNOSTICS GMBH
Country
GERMANY
Authorized Representative