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40410LG

by Karl Storz SE & CO. KG

Ref 40410LG

40410LG is a Class I device made by Karl Storz SE & CO. KG, registered in EUDAMED on 19 May 2026 (Basic UDI-DI 4048551001174TM) and listed in FDA GUDID since 10 Jul 2025 (UDI-DI 04048551425763), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4048551001174TM Basic UDI-DI 04048551425763UDI-DIDate19 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04048551425763 UDI-DI Date10 Jul 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4048551001174TM registered 19 May 2026 Active
  • FDA GUDID UDI-DI 04048551425763 listed 10 Jul 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04048551425763
  2. Registered EUDAMED 4048551001174TM

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  • Withdrawn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

Generic name
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Device name
Dissectors, thoracic surgery
Model / Ref / Catalog
40410LG
Primary DI / UDI-DI
04048551425763
Basic UDI-DI
4048551001174TM
FDA product code
MDM
EMDN code
L080599 Thoracic surgery clamps, reusable - other
GMDN term
Surgical soft-tissue manipulation forceps, scissors-like, reusable
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 soft-tissue manipulation forceps, scissors-like, reusable

Similar devices in this category

Other devices filed under THORACIC SURGERY FORCEPS, REUSABLE.

Other devices from Karl Storz SE & CO. KG

See all devices from Karl Storz SE & CO. KG →

Properties

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