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Landanger J01449-22

by Landanger

Ref J01449-22Model MICROSURGERY FORCEPS, REUSABLE

Landanger J01449-22 is a Class I device made by Landanger, registered in EUDAMED on 16 Oct 2026 (Basic UDI-DI B-03661219435686) and listed in FDA GUDID since 25 Sep 2024 (UDI-DI 03661219435686), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-03661219435686 Basic UDI-DI 03661219435686UDI-DIDate16 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number03661219435686 UDI-DI Date25 Sep 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-03661219435686 registered 16 Oct 2026 Active
  • FDA GUDID UDI-DI 03661219435686 listed 25 Sep 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 03661219435686
  2. Registered EUDAMED B-03661219435686

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  • Withdrawn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
Landanger
Generic name
Surgical soft-tissue manipulation forceps, tweezers-like, reusable
Model / reference
J01449-22, MICROSURGERY FORCEPS, REUSABLE
Primary DI / UDI-DI
03661219435686
Basic UDI-DI
B-03661219435686
FDA product code
MDM
EMDN code
L1003 Microsurgery forceps, reusable
GMDN term
Surgical soft-tissue manipulation forceps, tweezers-like, reusable
Device class
Class I
Regulation number
878.4800
EU registration type
Legacy device (under a directive)
EU market of registration
France
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical soft-tissue manipulation forceps, tweezers-like, reusable

Similar devices in this category

Other devices filed under MICROSURGERY FORCEPS, REUSABLE.

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Properties

  • Sterilise before use
  • Reusable
  • Premarket exempt
  • Lot / batch number
Other properties (21, all answered No)