Journey E0015098-2
Journey E0015098-2 is a Class I device made by Smith & Nephew, Inc., listed in FDA GUDID since 24 Oct 2016 (UDI-DI 00885556663462), 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 | Number00885556663462 | Date24 Oct 2016 | StatusListed |
Official records
- AccessGUDID record 00885556663462
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Journey
- Generic name
- Bone approximation clamp
- Model / Ref / Catalog
- E0015098-2
- Primary DI / UDI-DI
- 00885556663462
- FDA product code
- LXH
- GMDN term
- Bone approximation clamp
- 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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