ACET2 - ARCSA Registration 66614cd162c46a1038dc009399fb4939
Access comprehensive regulatory information for ACET2 in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 66614cd162c46a1038dc009399fb4939 and manufactured by ROCHE DIAGNOSTICS GMBH. The device was registered on November 10, 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
66614cd162c46a1038dc009399fb4939
ACET2
ARCSA ID: 66614cd162c46a1038dc009399fb4939
Device Classification
Risk Class
III
Product Type
In Vitro Diagnostic
Brand Name
ROCHE
Commercial Name
17-408 IVD Reagents/Kits, Immunoassay, Toxicology
Registration Information
Analysis ID
66614cd162c46a1038dc009399fb4939
Registration Date
November 10, 2023
Expiration Date
November 10, 2028
Product Use
QUANTITATIVE DETERMINATION OF ACETAMINOPHEN (PARACETAMOL) OVERDOSE IN SERUM AND PLASMA.
Manufacturer
Product Owner
Name
ROCHE DIAGNOSTICS GMBH
Country
GERMANY
Authorized Representative