BF726
Part of a family of 6 devices: see the family page
Ref BF726Model Traction Device
BF726 is a Class I device made by Steris Corporation, registered in EUDAMED on 1 Oct 2026 (Basic UDI-DI 0724995MGTRACTIONDEVBA) and listed in FDA GUDID since 23 Apr 2021 (UDI-DI 00724995165352), active as of 7 Nov 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number0724995MGTRACTIONDEVBA 00724995165352 | Date1 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00724995165352 | Date23 Apr 2021 | StatusListed |
Official records
- EUDAMED public site 0724995MGTRACTIONDEVBA
- AccessGUDID record 00724995165352
Across registries
- EUDAMED Basic UDI-DI 0724995MGTRACTIONDEVBA registered 1 Oct 2026 Active
- FDA GUDID UDI-DI 00724995165352 listed 23 Apr 2021 Listed
Timeline
- Listed FDA GUDID 00724995165352
- Registered EUDAMED 0724995MGTRACTIONDEVBA
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Traction boot
- Device name
- Traction Device
- Model / Ref / Catalog
- BF726, Traction Device
- Description
- The Traction Boot Strap Set Contains two, 1.5 inch wide Strap and two, 2 inch wide Strap needed with TenZor Traction Unit.
- Primary DI / UDI-DI
- 00724995165352
- Basic UDI-DI
- 0724995MGTRACTIONDEVBA
- FDA product code
- HST
- EMDN code
- Z12130285 Orthopaedic traction instruments - consumables
- GMDN term
- Traction boot
- Device class
- Class I
- Regulation number
- 888.5850
- EU registration type
- Standard device
- EU market of registration
- Ireland
- GUDID distribution status
- In Commercial Distribution
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