MWD552
Ref MWD552Model 08858251027996VX
MWD552 is a Class I device made by Tornier, Inc., registered in EUDAMED on 13 Aug 2026 (Basic UDI-DI 08858251027996VX) and listed in FDA GUDID since 8 Aug 2022 (UDI-DI 03700386976742), 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 | Number08858251027996VX 03700386976742 | Date13 Aug 2026 | StatusActive |
| United States | GUDID listing GUDID | Number03700386976742 | Date8 Aug 2022 | StatusListed |
Official records
- EUDAMED public site 08858251027996VX
- AccessGUDID record 03700386976742
Across registries
- EUDAMED Basic UDI-DI 08858251027996VX registered 13 Aug 2026 Active
- FDA GUDID UDI-DI 03700386976742 listed 8 Aug 2022 Listed
Timeline
- Listed FDA GUDID 03700386976742
- Registered EUDAMED 08858251027996VX
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Aequalis® Reversed II
- Generic name
- Surgical torque wrench, reusable
- Device name
- Aequalis Reversed II Instrumentation - Screwdrivers AndTightening Instrumentation - Class I - Reusable - Non Sterile
- Model / Ref / Catalog
- MWD552, 08858251027996VX
- Primary DI / UDI-DI
- 03700386976742
- Basic UDI-DI
- 08858251027996VX
- Direct marketing DI
- 03700386976742
- FDA product code
- HXC
- EMDN code
- L091199 Orthopaedic prosthetics instruments, reusable - other
- GMDN term
- Surgical torque wrench, reusable
- Device class
- Class I
- Regulation number
- 888.4540
- 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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