BF001
BF001 is a Class I device made by Steris Corporation, listed in FDA GUDID since 23 Apr 2021 (UDI-DI 10724995191242), 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 | Number10724995191242 | Date23 Apr 2021 | StatusListed |
Official records
- AccessGUDID record 10724995191242
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Traction boot
- Model / Ref / Catalog
- BF001
- Primary DI / UDI-DI
- 10724995191242
- 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).
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- ACUMED 10170054 by ACUMED LLC
- ZEE TRACTION SPLINT by Zee Medical Products Co., Inc.
- BAC JAC by Haggin Industries, Inc.
- ACUMED 10100015 by ACUMED LLC
- MEDI-TRAK PORTABLE TRACTION DEVICE by Medicorp, Inc.
- TRACTION-STEEL FRAMING SYSTEM by Orthopedic Systems, Inc.
- BACK-ON-TRAC, MODEL 101BOT by Back-On-Track, Inc.