Devon 31145892
Ref 31145892
Devon 31145892 is a Class I device made by Cardinalhealth, registered in EUDAMED on 27 May 2026 (Basic UDI-DI B-10884521208742) and listed in FDA GUDID since 29 Jun 2018 (UDI-DI 10884521208742), active as of 23 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-10884521208742 10884521208742 | Date27 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number10884521208742 | Date29 Jun 2018 | StatusListed |
Official records
- EUDAMED public site B-10884521208742
- AccessGUDID record 10884521208742
Across registries
- EUDAMED Basic UDI-DI B-10884521208742 registered 27 May 2026 Active
- FDA GUDID UDI-DI 10884521208742 listed 29 Jun 2018 Listed
Timeline
- Listed FDA GUDID 10884521208742
- Registered EUDAMED B-10884521208742
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Devon
- Generic name
- Open-surgery electrosurgical electrode, monopolar, reusable
- Model / Ref / Catalog
- 31145892
- Primary DI / UDI-DI
- 10884521208742
- Basic UDI-DI
- B-10884521208742
- FDA product code
- FZZ
- EMDN code
- V9004 Skin marking dermographic pencils and pens
- GMDN term
- Open-surgery electrosurgical electrode, monopolar, reusable
- Device class
- Class I
- Regulation number
- 878.4660
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Ireland
- GUDID distribution status
- In Commercial Distribution
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