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Klappgriff+ mit Bodenstütze, glatt, 700mm

by Lehnen GmbH

Ref L1082001W, L1082001

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Overview

A medical device directory has listed the Klappgriff+ mit Bodenstütze, glatt, 700mm for safe and effective use in orthopedic procedures. This manual holds standard regulatory compliance, microbial substances, sutures, basic UDID data ULIDs, primary DI, implantable status, reprocesed status, actor names, version number, medical purpose, container packaging DIS, reusability, device name, statisusses, risk class ID, measuring function, actor names, near patient testing, status ID, sterilization, UDI UUID, special device type ID, abbreviated actor names, MF SRN, trade name, companion diagnostics, sterile status, professional testing, MF name, new device, endocrine disruptor, kit, lateX, device model, and MF actor names.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4250365200001QJ Basic UDI-DI Date5 Jul 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Haltegriff glatt 300mm
Model / Reference
L1082001W, L1082001
Primary DI / UDI-DI
04250365218183, 04250365218176
Basic UDI-DI
4250365200001QJ
Direct Marketing DI
04250365218183
04250365218176
EMDN Code
Y181806 Handles
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000025229

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Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No