BF00023
BF00023 is a traction boot (FDA Class I; FDA product code HST, Apparatus, traction, non-powered) made by Steris Corporation, listed in FDA GUDID since 23 Apr 2021 (UDI-DI 00724995191207), registry data as of 22 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 | Number00724995191207 | Date23 Apr 2021 | StatusListed |
Official records
- AccessGUDID record 00724995191207
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Traction boot
- Model / Ref / Catalog
- BF00023
- Primary DI / UDI-DI
- 00724995191207
- FDA product code
- HST
- GMDN term
- Traction boot
- Device class
- Class I
- Regulation number
- 888.5850
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code HST (Apparatus, traction, non-powered).
- TRACTION ACCESSORIES by Danek Medical, Inc.
- NECKTRAC by Lossing Orthopedic, Inc.
- ACUMED 10150143 by ACUMED LLC
- ACUMED 10170052 by ACUMED LLC
- EXTREMITY ELEVATOR by Orthopedic Systems, Inc.
- COTTRELL 90/90 BACKTRAC by Lossing Orthopedic, Inc.
- BACK TRAC by Tech Engineering, Inc.
- ACUFEX SHOULDER HOLDER by Acufex Microsurgical, Inc.
- NEC-KRADLE BY VENCOR by Vencor
- PROT-A-TRAC by Robert I. Branick, M.D.