Phosphorus
Ref PHOS-0230, PHOS-0600
Phosphorus (PHOS-0230) is an in vitro diagnostic device (EU IVDR Class B) made by Vitalscientific, registered in EUDAMED on 10 Sep 2025 (Basic UDI-DI 37017008PHOS00DL) and listed in FDA GUDID since 31 Mar 2025 (UDI-DI 03701700825500), active as of 22 Oct 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 | Number37017008PHOS00DL | Date10 Sep 2025 | StatusActive |
| United States | GUDID listing GUDID | Number03701700825500 | Date31 Mar 2025 | StatusListed |
Official records
- EUDAMED public site 37017008PHOS00DL
- AccessGUDID record 03701700825500
Across registries
- EUDAMED Basic UDI-DI 37017008PHOS00DL registered 10 Sep 2025 Active
- FDA GUDID UDI-DI 03701700825500 listed 31 Mar 2025 Listed
Timeline
- Listed FDA GUDID 03701700825500
- Registered EUDAMED 37017008PHOS00DL
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Inorganic phosphate (PO43-) IVD, kit, spectrophotometry
- Model / reference
- PHOS-0230, PHOS-0600
- Primary DI / UDI-DI
- 03701700825500, 03701700825609
- Basic UDI-DI
- 37017008PHOS00DL
- EMDN code
- W01010307 Phosphate inorganic / phosphorus
- GMDN term
- Inorganic phosphate (PO43-) IVD, kit, spectrophotometry
- Device class
- Class B
- EU registration type
- Standard device
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
Manufacturer details
- EUDAMED SRN
- FR-MF-000004722
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