Freezer Ring ASB0050
by Tecres
Ref ASB0050
Freezer Ring ASB0050 is a Class I device made by Tecres, registered in EUDAMED on 29 Sep 2026 (Basic UDI-DI 80314970612P3) and listed in FDA GUDID since 23 Sep 2022 (UDI-DI 08031497001999), active as of 25 Oct 2026.
Active
CE MDR
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/MDR EUDAMED | Number80314970612P3 08031497001999 | Date29 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number08031497001999 | Date23 Sep 2022 | StatusListed |
Official records
- EUDAMED public site 80314970612P3
- AccessGUDID record 08031497001999
Across registries
- EUDAMED Basic UDI-DI 80314970612P3 registered 29 Sep 2026 Active
- FDA GUDID UDI-DI 08031497001999 listed 23 Sep 2022 Listed
Timeline
- Listed FDA GUDID 08031497001999
- Registered EUDAMED 80314970612P3
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Freezer Ring
- Generic name
- Orthopaedic cement-chilling device
- Model / reference
- ASB0050
- Primary DI / UDI-DI
- 08031497001999
- Basic UDI-DI
- 80314970612P3
- FDA product code
- KDD
- EMDN code
- K010399 Spinal endotherapy devices - other
- GMDN term
- Orthopaedic cement-chilling device
- Device class
- Class I
- Regulation number
- 878.4800
- EU registration type
- Standard device
- EU market of registration
- Italy
- GUDID distribution status
- In Commercial Distribution
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