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Devon 31145892

by Cardinalhealth

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 European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10884521208742 Basic UDI-DI 10884521208742UDI-DIDate27 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10884521208742 UDI-DI Date29 Jun 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10884521208742 registered 27 May 2026 Active
  • FDA GUDID UDI-DI 10884521208742 listed 29 Jun 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10884521208742
  2. Registered EUDAMED B-10884521208742

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

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

Similar devices in this category

Other devices filed under SKIN MARKING DERMOGRAPHIC PENCILS AND PENS.

Other devices from Cardinalhealth

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Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)