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Landanger B50220

by Landanger

Ref B50220Model GRASPING FORCEPS, REUSABLE

Landanger B50220 is a Class I device made by Landanger, registered in EUDAMED on 15 Oct 2026 (Basic UDI-DI B-03661219007715) and listed in FDA GUDID since 1 Apr 2024 (UDI-DI 03661219007715), 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-03661219007715 Basic UDI-DI 03661219007715UDI-DIDate15 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number03661219007715 UDI-DI Date1 Apr 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-03661219007715 registered 15 Oct 2026 Active
  • FDA GUDID UDI-DI 03661219007715 listed 1 Apr 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 03661219007715
  2. Registered EUDAMED B-03661219007715

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  • Withdrawn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, scissors-like, reusable
Model / reference
B50220, GRASPING FORCEPS, REUSABLE
Primary DI / UDI-DI
03661219007715
Basic UDI-DI
B-03661219007715
FDA product code
DWS
EMDN code
L03130401 Tissue and organ grasping forceps, reusable
GMDN term
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Device class
Class I
Regulation number
870.4500
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, scissors-like, reusable

Similar devices in this category

Other devices filed under TISSUE AND ORGAN GRASPING FORCEPS, REUSABLE.

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Properties

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