Tornier Perform MWH712S
Tornier Perform MWH712S is a Class I device made by Tornier, Inc., listed in FDA GUDID since 10 Aug 2022 (UDI-DI 00846832070022), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00846832070022 | Date10 Aug 2022 | StatusListed |
Official records
- AccessGUDID record 00846832070022
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Tornier Perform
- Generic name
- Shoulder glenoid fossa prosthesis trial
- Model / Ref / Catalog
- MWH712S
- Primary DI / UDI-DI
- 00846832070022
- FDA product code
- LXH
- GMDN term
- Shoulder glenoid fossa prosthesis trial
- Device class
- Class I
- Regulation number
- 888.4540
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Angle — 25 degree
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