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Loqteq® Ic 6944-31

by aap Implantate AG

Ref IC 6944-31Model Instrument

Loqteq® Ic 6944-31 is a Class I device made by aap Implantate AG, registered in EUDAMED on 29 May 2026 (Basic UDI-DI 40424090079HL) and listed in FDA GUDID since 28 Feb 2018 (UDI-DI 04042409260568), active as of 23 Oct 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number40424090079HL Basic UDI-DI 04042409260568UDI-DIDate29 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04042409260568 UDI-DI Date28 Feb 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 40424090079HL registered 29 May 2026 Active
  • FDA GUDID UDI-DI 04042409260568 listed 28 Feb 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04042409260568
  2. Registered EUDAMED 40424090079HL

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  • Withdrawn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
Loqteq®
Generic name
Surgical instrument/implant rack
Model / reference
IC 6944-31, Instrument
Primary DI / UDI-DI
04042409260568
Basic UDI-DI
40424090079HL
FDA product code
FSM
EMDN code
V0402 Clinical use trays and bowls
GMDN term
Surgical instrument/implant rack
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical instrument/implant rack

Other devices from aap Implantate AG

See all devices from aap Implantate AG →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)