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Aesculap

by Aesculap AG 1,000+ variants

Part of a family of 8 devices: see the family page

Ref LX618R

Aesculap (LX618R) is a Class I device made by Aesculap AG, registered in EUDAMED on 19 Jan 2026 (Basic UDI-DI 40392390000006272H) and listed in FDA GUDID since 8 May 2020 (UDI-DI 04038653050383), 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 Number40392390000006272H Basic UDI-DI 04038653050383UDI-DIDate19 Jan 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04038653050383 UDI-DI Date8 May 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 40392390000006272H registered 19 Jan 2026 Active
  • FDA GUDID UDI-DI 04038653050383 listed 8 May 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04038653050383
  2. Registered EUDAMED 40392390000006272H

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  • Withdrawn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 flat-nosed pliers
Device name
Plaster instrument
Model / Ref / Catalog
LX618R
Primary DI / UDI-DI
04038653050383
Basic UDI-DI
40392390000006272H
Direct marketing DI
04038653050383
FDA product code
LGG
EMDN code
Z12139099 Various orthopaedic and traumatology instruments - other
GMDN term
Surgical flat-nosed pliers
Device class
Class I
Regulation number
888.5980
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Manufacturer details

EUDAMED SRN
DE-MF-000005504

Similar devices in this category

Other devices filed under VARIOUS ORTHOPAEDIC AND TRAUMATOLOGY INSTRUMENTS - OTHER.

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Properties

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