Journey 74031247
Journey 74031247 is a Class I device made by Smith & Nephew, Inc., listed in FDA GUDID since 30 Sep 2021 (UDI-DI 00885556786895), 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 | Number00885556786895 | Date30 Sep 2021 | StatusListed |
Official records
- AccessGUDID record 00885556786895
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Journey
- Generic name
- Knee tibia prosthesis trial, reusable
- Model / Ref / Catalog
- 74031247
- Description
- JOURNEY II ARTICULAR STABILIZED ARTICULAR INSERT TRIAL SIZE 7-8 LEFT 9MM
- Primary DI / UDI-DI
- 00885556786895
- FDA product code
- HWT
- GMDN term
- Knee tibia prosthesis trial, reusable
- Device class
- Class I
- Regulation number
- 888.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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