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Clickline 31110EH

by Karl Storz SE & CO. KG

Part of a family of 7 devices: see the family page

Ref 31110EH

Clickline 31110EH is a device classified as Class IIb in the EU and Class II in the US made by Karl Storz SE & CO. KG, registered in EUDAMED on 19 May 2026 (Basic UDI-DI 4048551000451TH) and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04048551333846), active as of 7 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4048551000451TH Basic UDI-DI 04048551333846UDI-DIDate19 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04048551333846 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4048551000451TH registered 19 May 2026 Active
  • FDA GUDID UDI-DI 04048551333846 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04048551333846
  2. Registered EUDAMED 4048551000451TH

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  • Withdrawn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
Clickline
Generic name
Rigid endoscopic scissors, reusable
Device name
HF scissor inserts
Model / reference
31110EH
Primary DI / UDI-DI
04048551333846
Basic UDI-DI
4048551000451TH
FDA product code
GCJ
EMDN code
Z12010980 Electrosurgery instruments - hardware accessories
GMDN term
Rigid endoscopic scissors, reusable
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
876.1500
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II

Device class is stated on each registry's own scale: Class IIb in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Rigid endoscopic scissors, reusable

Similar devices in this category

Other devices filed under ELECTROSURGERY INSTRUMENTS - HARDWARE ACCESSORIES.

Other devices from Karl Storz SE & CO. KG

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

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (22, all answered No)