Vitros 6844463
Ref 6844463Model VITROS
Vitros 6844463 is a device classified as Class A in the EU and Class I in the US made by Ortho-Clinical Diagnostics, registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI 10758750031672M3) and listed in FDA GUDID since 12 May 2023 (UDI-DI 10758750031672), active as of 7 Nov 2026.
Active
CE IVDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/IVDR EUDAMED | Number10758750031672M3 10758750031672 | Date30 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number10758750031672 | Date12 May 2023 | StatusListed |
Official records
- EUDAMED public site 10758750031672M3
- AccessGUDID record 10758750031672
Across registries
- EUDAMED Basic UDI-DI 10758750031672M3 registered 30 Oct 2026 Active
- FDA GUDID UDI-DI 10758750031672 listed 12 May 2023 Listed
Timeline
- Listed FDA GUDID 10758750031672
- Registered EUDAMED 10758750031672M3
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- VITROS Chemistry Products Electrolyte Reference Fluid (ERF) 800 EUDAMEDVitros GUDID
- Generic name
- Buffered wash solution IVD
- Model / Ref / Catalog
- 6844463, VITROS
- Primary DI / UDI-DI
- 10758750031672
- Basic UDI-DI
- 10758750031672M3
- FDA product code
- PPM
- EMDN code
- W0201010185 Chemistry analysers - consumables
- GMDN term
- Buffered wash solution IVD
- Device class
- Class A EUDAMEDClass I GUDID
- Regulation number
- 864.4010
- EU registration type
- Standard device
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class A | Class I |
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