fa51e872f97de3321f2dc2427bcf2050
DIBU
ROCHE DIAGNOSTICS GMBH·III·Ecuador ARCSA·Registered September 03, 2023
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
Manufacturer
- City
- MANNHEIM
- Country
- GERMANY
- Address
- SANDHOFER STR. 116, 68305 MANNHEIM
Product owner
- Name
- ROCHE DIAGNOSTICS GMBH
- Country
- GERMANY
Authorized representative
- Address
- AV SIMON BOLIVAR N/A Y VIA A NAYON
- Phone
- 3997100
Product use
IN VITRO DETERMINATION OF DIBUCAINE NUMBER FOR USE WITH THE CHOLINESTERASE IN VITRO TEST.
About this record
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.