Truliant 02-029-25-3445
Truliant 02-029-25-3445 is a Class I device made by Exactech, Inc., listed in FDA GUDID since 25 Aug 2022 (UDI-DI 10885862556653), 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 | Number10885862556653 | Date25 Aug 2022 | StatusListed |
Official records
- AccessGUDID record 10885862556653
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Truliant
- Generic name
- Knee tibia prosthesis trial, reusable
- Model / Ref / Catalog
- 02-029-25-3445
- Primary DI / UDI-DI
- 10885862556653
- 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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