7000 Series Leg Section
by Steris Corporation 5 variants
Ref BF00217Model Leg Positioner
7000 Series Leg Section (BF00217) is a Class I device made by Steris Corporation, registered in EUDAMED on 25 Sep 2026 (Basic UDI-DI 0724995MG7000LEGPSTNRGQ) and listed in FDA GUDID since 8 Mar 2024 (UDI-DI 00724995229269), active as of 25 Oct 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 | Number0724995MG7000LEGPSTNRGQ 00724995229269 | Date25 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00724995229269 | Date8 Mar 2024 | StatusListed |
Official records
- EUDAMED public site 0724995MG7000LEGPSTNRGQ
- AccessGUDID record 00724995229269
Across registries
- EUDAMED Basic UDI-DI 0724995MG7000LEGPSTNRGQ registered 25 Sep 2026 Active
- FDA GUDID UDI-DI 00724995229269 listed 8 Mar 2024 Listed
Timeline
- Listed FDA GUDID 00724995229269
- Registered EUDAMED 0724995MG7000LEGPSTNRGQ
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Leg procedure positioner
- Device name
- Leg Positioner
- Model / Ref / Catalog
- Leg Positioner, BF00217, 7000 Series Leg Section
- Primary DI / UDI-DI
- 00724995229269
- Basic UDI-DI
- 0724995MG7000LEGPSTNRGQ
- FDA product code
- BWN
- EMDN code
- Z12011299 Patient positioning instruments – other
- GMDN term
- Leg procedure positioner
- Device class
- Class I
- Regulation number
- 878.4950
- EU registration type
- Standard device
- EU market of registration
- Ireland
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | Leg Positioner BF00217 | 7000 Series Leg Section |
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