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Gimmi KN.1464.20

by Gimmi GmbH

Ref KN.1464.20

Gimmi KN.1464.20 is a Class I device made by Gimmi GmbH, registered in EUDAMED on 8 Sep 2026 (Basic UDI-DI B-04049047061465) and listed in FDA GUDID since 20 May 2025 (UDI-DI 04049047061465), 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-04049047061465 Basic UDI-DI 04049047061465UDI-DIDate8 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04049047061465 UDI-DI Date20 May 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04049047061465 registered 8 Sep 2026 Active
  • FDA GUDID UDI-DI 04049047061465 listed 20 May 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04049047061465
  2. Registered EUDAMED B-04049047061465

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  • Withdrawn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
Gimmi
Generic name
Bone file/rasp, manual, reusable
Device name
Lambotte Raspatory
Model / Ref / Catalog
KN.1464.20
Description
LAMBOTTE RASPATORY 20 MM LENGTH 210 MM
Primary DI / UDI-DI
04049047061465
Basic UDI-DI
B-04049047061465
FDA product code
LXH
EMDN code
L091201 Orthopaedic surgery rasps, reusable
GMDN term
Bone file/rasp, manual, reusable
Device class
Class I
Regulation number
888.4540
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone file/rasp, manual, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY RASPS, REUSABLE.

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Properties

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