Profix 71517522
Profix 71517522 is a Class I device made by Smith & Nephew, Inc., listed in FDA GUDID since 28 Sep 2015 (UDI-DI 03596010540232), 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 | Number03596010540232 | Date28 Sep 2015 | StatusListed |
Official records
- AccessGUDID record 03596010540232
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Profix
- Generic name
- Knee tibia prosthesis trial, reusable
- Model / Ref / Catalog
- 71517522
- Primary DI / UDI-DI
- 03596010540232
- FDA product code
- LXH
- GMDN term
- Knee tibia prosthesis trial, reusable
- 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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