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Aesculap LX165R

by Aesculap AG

Part of a family of 15 devices: see the family page

Ref LX165R

Aesculap LX165R is a Class I device made by Aesculap AG, registered in EUDAMED on 16 Sep 2025 (Basic UDI-DI 403923900000033827) and listed in FDA GUDID since 8 May 2020 (UDI-DI 04038653079483), active as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number403923900000033827 Basic UDI-DI 04038653079483UDI-DIDate16 Sep 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04038653079483 UDI-DI Date8 May 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 403923900000033827 registered 16 Sep 2025 Active
  • FDA GUDID UDI-DI 04038653079483 listed 8 May 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04038653079483
  2. Registered EUDAMED 403923900000033827

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  • Withdrawn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

Trade name
Aesculap
Generic name
Orthopaedic implantable-device cutter
Model / Ref / Catalog
LX165R
Primary DI / UDI-DI
04038653079483
Basic UDI-DI
403923900000033827
Direct marketing DI
04038653079483
FDA product code
HXZ
EMDN code
L01041202 Wires and metal plates scissors, reusable
GMDN term
Orthopaedic implantable-device cutter
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)