66614cd162c46a1038dc009399fb4939
ACET2
ROCHE DIAGNOSTICS GMBH·III·Ecuador ARCSA·Registered November 10, 2023
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
Manufacturer
- City
- MANNHEIM
- Country
- GERMANY
- Address
- SANDHOFER STR. 116
Product owner
- Name
- ROCHE DIAGNOSTICS GMBH
- Country
- GERMANY
Authorized representative
- Address
- AV SIMON BOLIVAR N/A Y VIA A NAYON
- Phone
- 3997100
Product use
QUANTITATIVE DETERMINATION OF ACETAMINOPHEN (PARACETAMOL) OVERDOSE IN SERUM AND PLASMA.
About this record
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.