Imaging Extension
by Steris Corporation 3 variants
Part of a family of 12 devices: see the family page
Ref BF00317Model Orthopaedic Extension
Imaging Extension (BF00317) is a Class I device made by Steris Corporation, registered in EUDAMED on 25 Sep 2026 (Basic UDI-DI 0724995MG7000ORTHOEXTRS) and listed in FDA GUDID since 24 Apr 2025 (UDI-DI 00724995231040), active as of 23 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 | Number0724995MG7000ORTHOEXTRS 00724995231040 | Date25 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00724995231040 | Date24 Apr 2025 | StatusListed |
Official records
- EUDAMED public site 0724995MG7000ORTHOEXTRS
- AccessGUDID record 00724995231040
Across registries
- EUDAMED Basic UDI-DI 0724995MG7000ORTHOEXTRS registered 25 Sep 2026 Active
- FDA GUDID UDI-DI 00724995231040 listed 24 Apr 2025 Listed
Timeline
- Listed FDA GUDID 00724995231040
- Registered EUDAMED 0724995MG7000ORTHOEXTRS
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Universal operating table top
- Device name
- Orthopaedic Extension
- Model / Ref / Catalog
- Orthopaedic Extension, BF00317, Imaging Extension
- Primary DI / UDI-DI
- 00724995231040
- Basic UDI-DI
- 0724995MG7000ORTHOEXTRS
- FDA product code
- FQO
- EMDN code
- Z12011299 Patient positioning instruments – other
- GMDN term
- Universal operating table top
- Device class
- Class I
- Regulation number
- 878.4960
- EU registration type
- Standard device
- EU market of registration
- Ireland
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | Orthopaedic Extension BF00317 | Imaging Extension |
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