Fujifilm St-10
Ref 04547410228090
Fujifilm St-10 is a Class I device made by Fujifilm Corporation, registered in EUDAMED on 23 Oct 2026 (Basic UDI-DI 454741020100000000000545C) and listed in FDA GUDID since 7 Oct 2022 (UDI-DI 04547410228090), 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 | Number454741020100000000000545C 04547410228090 | Date23 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04547410228090 | Date7 Oct 2022 | StatusListed |
Official records
- EUDAMED public site 454741020100000000000545C
- AccessGUDID record 04547410228090
Across registries
- EUDAMED Basic UDI-DI 454741020100000000000545C registered 23 Oct 2026 Active
- FDA GUDID UDI-DI 04547410228090 listed 7 Oct 2022 Listed
Timeline
- Listed FDA GUDID 04547410228090
- Registered EUDAMED 454741020100000000000545C
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Setting tool ST-10 EUDAMEDFujifilm GUDID
- Generic name
- Endoscope balloon positioner, reusable
- Device name
- Setting tool 3
- Model / reference
- 04547410228090 EUDAMEDST-10 GUDID
- Primary DI / UDI-DI
- 04547410228090
- Basic UDI-DI
- 454741020100000000000545C
- Direct marketing DI
- 04547410228090
- FDA product code
- FFY
- EMDN code
- Z12029099 Various instruments for endoscopy and mini–invasive surgery – other
- GMDN term
- Endoscope balloon positioner, reusable
- Device class
- Class I
- Regulation number
- 876.1500
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 04547410228090 | ST-10 |
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