Mini Wright 3104124
by Clement Clarke International Limited
Ref 3104124
Mini Wright 3104124 is a device classified as Class I in the EU and Class II in the US made by Clement Clarke International Limited, registered in EUDAMED on 17 Aug 2026 (Basic UDI-DI B-05023323000941) and listed in FDA GUDID since 7 Sep 2016 (UDI-DI 05023323000941), active as of 22 Oct 2026.
Active
CE MDD
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/MDD EUDAMED | NumberB-05023323000941 05023323000941 | Date17 Aug 2026 | StatusActive |
| United States | GUDID listing GUDID | Number05023323000941 | Date7 Sep 2016 | StatusListed |
Official records
- EUDAMED public site B-05023323000941
- AccessGUDID record 05023323000941
Across registries
- EUDAMED Basic UDI-DI B-05023323000941 registered 17 Aug 2026 Active
- FDA GUDID UDI-DI 05023323000941 listed 7 Sep 2016 Listed
Timeline
- Listed FDA GUDID 05023323000941
- Registered EUDAMED B-05023323000941
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Flexicare EUDAMEDMini Wright GUDID
- Generic name
- Expiratory peak flow meter, analogue, reusable
- Device name
- PFM and Mouthpieces
- Model / Ref / Catalog
- 3104124
- Primary DI / UDI-DI
- 05023323000941
- Basic UDI-DI
- B-05023323000941
- FDA product code
- BZH
- EMDN code
- R900902 Inspiratory and expiratory flow stimulators/respiratory muscles trainers
- GMDN term
- Expiratory peak flow meter, analogue, reusable
- Device class
- Class I EUDAMEDClass II GUDID
- Regulation number
- 868.1860
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Northern Ireland
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class I | Class II |
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