c1ade292661f5e5e94fbe4026b4cbda2
A1CD2
ROCHE DIAGNOSTICS GMBH·II·Ecuador ARCSA·Registered November 27, 2023
Device classification
- Risk class
- II
- Product type
- In Vitro Diagnostic
- Brand name
- ROCHE
- Commercial name
- 18-904 IVD Reagents/Test Kits, Clinical Chemistry, Protein, Glycosylated, Hemoglobin
Registration information
- Analysis ID
- c1ade292661f5e5e94fbe4026b4cbda2
- Registration date
- November 27, 2023
- Expiration date
- November 27, 2028
Manufacturer
- City
- MANNHEIM
- Country
- GERMANY
- Address
- SANDHOFER STRASSE 11668305 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
DILUYENTE OF THE TIN-QUANT HEMOGLOBIN A1C TEST.
About this record
Access comprehensive regulatory information for A1CD2 in the Ecuador medical device market through Pure Global AI's free database. This II medical device is registered under ARCSA ID c1ade292661f5e5e94fbe4026b4cbda2 and manufactured by ROCHE DIAGNOSTICS GMBH. The device was registered on November 27, 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.