Case Lid 110031221
Ref 110031221
Case Lid 110031221 is a Class I device made by Biomet Orthopedics, Inc., registered in EUDAMED on 31 Oct 2026 (Basic UDI-DI 889024AR2ZB) and listed in FDA GUDID since 22 Apr 2022 (UDI-DI 00880304830158), active as of 7 Nov 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 | Number889024AR2ZB 00880304830158 | Date31 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00880304830158 | Date22 Apr 2022 | StatusListed |
Official records
- EUDAMED public site 889024AR2ZB
- AccessGUDID record 00880304830158
Across registries
- EUDAMED Basic UDI-DI 889024AR2ZB registered 31 Oct 2026 Active
- FDA GUDID UDI-DI 00880304830158 listed 22 Apr 2022 Listed
Timeline
- Listed FDA GUDID 00880304830158
- Registered EUDAMED 889024AR2ZB
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Case Lid
- Generic name
- Instrument tray, reusable
- Device name
- Stainless Steel Lid
- Model / Ref / Catalog
- 110031221
- Primary DI / UDI-DI
- 00880304830158
- Basic UDI-DI
- 889024AR2ZB
- Direct marketing DI
- 00880304830158
- FDA product code
- FSM
- EMDN code
- L99 Surgical instruments, reusable - other
- GMDN term
- Instrument tray, reusable
- Device class
- Class I
- Regulation number
- 878.4800
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under SURGICAL INSTRUMENTS, REUSABLE - OTHER.