Skip to content

Spex Limited 1156-0301-210-L

by Spex Limited

Ref 1156-0301-210-L

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

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number94200517ARMTHIGHCOMBOPF Basic UDI-DI 09420082646643UDI-DIDate11 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number09420082646643 UDI-DI Date7 Nov 2025ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

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  • Withdrawn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
Spex EUDAMED
Spex Limited GUDID
Generic Name
Wheelchair/chair/stander occupant restraint/support
Device Name
Arm and Thigh Combination Support
Model / Reference
1156-0301-210-L
Primary DI / UDI-DI
09420082646643
Basic UDI-DI
94200517ARMTHIGHCOMBOPF
FDA Product Code
KNN
EMDN Code
Y122406 Belts, seats and armrests for wheelchairs
GMDN Term
Wheelchair/chair/stander occupant restraint/support
Device Class
Class I
Regulation Number
890.3920
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Other devices from Spex Limited

See all devices from Spex Limited →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (21)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No