Reunion 5901-1240
by Stryker GmbH
Reunion 5901-1240 is a Class I device made by Stryker GmbH, listed in FDA GUDID since 24 Sep 2018 (UDI-DI 07613327099058), registry data as of 12 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07613327099058 | Date24 Sep 2018 | StatusListed |
Official records
- AccessGUDID record 07613327099058
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Reunion
- Generic name
- Shoulder glenoid fossa prosthesis trial
- Model / Ref / Catalog
- 5901-1240
- Primary DI / UDI-DI
- 07613327099058
- 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
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