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Footsure 60250

by Therafin Corporation

Ref 60250

Footsure 60250 is a Class I device made by Therafin Corporation, registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI 0840252960250U4) and listed in FDA GUDID since 10 Sep 2026 (UDI-DI 00840252901584), active as of 7 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0840252960250U4 Basic UDI-DI 00840252901584UDI-DIDate4 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00840252901584 UDI-DI Date10 Sep 2026ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0840252960250U4 registered 4 Nov 2026 Active
  • FDA GUDID UDI-DI 00840252901584 listed 10 Sep 2026 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00840252901584
  2. Registered EUDAMED 0840252960250U4

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Footsure Ankle Support with Buckle, X-Small Pair EUDAMED
Footsure GUDID
Generic name
Wheelchair footrest/legrest
Model / Ref / Catalog
60250
Primary DI / UDI-DI
00840252901584
Basic UDI-DI
0840252960250U4
FDA product code
KNO
EMDN code
Y122403 Wheelchair footrests, supports and controls
GMDN term
Wheelchair footrest/legrest
Device class
Class I
Regulation number
890.3910
EU registration type
Standard device
EU market of registration
France
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under WHEELCHAIR FOOTRESTS, SUPPORTS AND CONTROLS.

Other devices from Therafin Corporation

See all devices from Therafin Corporation →

Properties

  • Premarket exempt
  • Manufacturing date
Other properties (23, all answered No)