Glucose
Ref 1419-0012, 1415-0012, 1419-0018, 1417-0017, 1418-0017
Glucose (1419-0012) is a glucose IVD (EU IVDR Class C) made by Medicon Hellas SA, registered in EUDAMED on 28 Dec 2022 (Basic UDI-DI 5204309000025NS) and listed in FDA GUDID since 27 Apr 2026 (UDI-DI 05204309087303), 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 | Number05204309087303 | Date27 Apr 2026 | StatusListed |
| European Union | CE/IVDR EUDAMED | Number5204309000025NS | Date28 Dec 2022 | StatusActive |
Official records
- EUDAMED public site 5204309000025NS
- AccessGUDID record 05204309123421
- AccessGUDID record 05204309039791
Across registries
- EUDAMED Basic UDI-DI 5204309000025NS registered 28 Dec 2022 Active
- FDA GUDID UDI-DI 05204309087303 listed 27 Apr 2026 Listed
Timeline
- Registered EUDAMED 5204309000025NS
- Listed FDA GUDID 05204309087303
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Glucose IVD, kit, spectrophotometry
- Model / Ref / Catalog
- 1419-0012, 1415-0012, 1419-0018, 1417-0017, 1418-0017
- Primary DI / UDI-DI
- 05204309087303, 05204309171491, 05204309123421, 05204309136650, 05204309039791
- Basic UDI-DI
- 5204309000025NS
- Direct marketing DI
- 0520430908730305204309171491052043091234210520430913665005204309039791
- EMDN code
- W01010213 Glucose
- GMDN term
- Glucose IVD, kit, spectrophotometry
- Device class
- Class C
- 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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