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Landanger B807672

by Landanger

Ref B807672Model SELF-STATIC RETRACTING DEVICES, REUSABLE

Landanger B807672 is a Class I device made by Landanger, registered in EUDAMED on 15 Oct 2026 (Basic UDI-DI B-03661219466031) and listed in FDA GUDID since 19 Jan 2026 (UDI-DI 03661219466031), 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-03661219466031 Basic UDI-DI 03661219466031UDI-DIDate15 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number03661219466031 UDI-DI Date19 Jan 2026ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-03661219466031 registered 15 Oct 2026 Active
  • FDA GUDID UDI-DI 03661219466031 listed 19 Jan 2026 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 03661219466031
  2. Registered EUDAMED B-03661219466031

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  • Withdrawn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
Self-retaining surgical retractor, reusable
Model / reference
B807672, SELF-STATIC RETRACTING DEVICES, REUSABLE
Primary DI / UDI-DI
03661219466031
Basic UDI-DI
B-03661219466031
FDA product code
GAD
EMDN code
L03140101 Self-static spreaders, reusable
GMDN term
Self-retaining surgical retractor, 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

Similar devices in this category

Other devices filed under GENERAL SURGERY INSTRUMENTS, REUSABLE.

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Properties

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