Phosphorus
by Medicon Hellas SA 2 variants
Ref 1415-0210, 1419-0212
Phosphorus (1415-0210) is an in vitro diagnostic device (EU IVDR Class B) made by Medicon Hellas SA, registered in EUDAMED on 20 Sep 2023 (Basic UDI-DI 5204309000038P3) and listed in FDA GUDID since 27 Apr 2026 (UDI-DI 05204309167388), 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 |
|---|---|---|---|---|
| United States | GUDID listing GUDID | Number05204309167388 | Date27 Apr 2026 | StatusListed |
| European Union | CE/IVDR EUDAMED | Number5204309000038P3 | Date20 Sep 2023 | StatusActive |
Official records
- EUDAMED public site 5204309000038P3
- AccessGUDID record 05204309087365
Across registries
- EUDAMED Basic UDI-DI 5204309000038P3 registered 20 Sep 2023 Active
- FDA GUDID UDI-DI 05204309167388 listed 27 Apr 2026 Listed
Timeline
- Registered EUDAMED 5204309000038P3
- Listed FDA GUDID 05204309167388
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Inorganic phosphate (PO43-) IVD, reagent
- Model / Ref / Catalog
- 1415-0210, 1419-0212
- Primary DI / UDI-DI
- 05204309167388, 05204309087365
- Basic UDI-DI
- 5204309000038P3
- EMDN code
- W01010307 Phosphate inorganic / phosphorus
- GMDN term
- Inorganic phosphate (PO43-) IVD, reagent
- Device class
- Class B
- EU registration type
- Standard device
- EU market of registration
- Greece
- GUDID distribution status
- In Commercial Distribution
Manufacturer details
- EUDAMED SRN
- GR-MF-000013625
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