44132006
by Wright Medical Technology, Inc.
Ref 44132006Model 08858251028145UD
44132006 is a Class I device made by Wright Medical Technology, Inc., registered in EUDAMED on 26 Oct 2026 (Basic UDI-DI 08858251028145UD) and listed in FDA GUDID since 8 Dec 2023 (UDI-DI 00889797109758), 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 | Number08858251028145UD 00889797109758 | Date26 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00889797109758 | Date8 Dec 2023 | StatusListed |
Official records
- EUDAMED public site 08858251028145UD
- AccessGUDID record 00889797109758
Across registries
- EUDAMED Basic UDI-DI 08858251028145UD registered 26 Oct 2026 Active
- FDA GUDID UDI-DI 00889797109758 listed 8 Dec 2023 Listed
Timeline
- Listed FDA GUDID 00889797109758
- Registered EUDAMED 08858251028145UD
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Charlotte®
- Generic name
- Instrument tray, reusable
- Device name
- Charlotte Muc Screw Instrumentation - Trays and Tray Accessories - Class I - Nonsterile
- Model / Ref / Catalog
- 44132006, 08858251028145UD
- Primary DI / UDI-DI
- 00889797109758
- Basic UDI-DI
- 08858251028145UD
- Direct marketing DI
- 00889797109758
- FDA product code
- LRP
- EMDN code
- L098099 Orthopaedic and traumatological surgery instruments, reusable - other accessories
- 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
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