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Clickline 26310

by Karl Storz SE & CO. KG

Ref 26310

Clickline 26310 is a Class I device made by Karl Storz SE & CO. KG, registered in EUDAMED on 19 May 2026 (Basic UDI-DI 4048551000697UK) and listed in FDA GUDID since 28 Mar 2025 (UDI-DI 04048551426852), 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 Number4048551000697UK Basic UDI-DI 04048551426852UDI-DIDate19 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04048551426852 UDI-DI Date28 Mar 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4048551000697UK registered 19 May 2026 Active
  • FDA GUDID UDI-DI 04048551426852 listed 28 Mar 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04048551426852
  2. Registered EUDAMED 4048551000697UK

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  • Withdrawn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
Surgical instrument handle, non-torque-limiting
Device name
Instrument handles, gynecology
Model / Ref / Catalog
26310
Primary DI / UDI-DI
04048551426852
Basic UDI-DI
4048551000697UK
FDA product code
NWW
EMDN code
Z12080280 Gynaecology and fertility treatment instruments - hardware accessories
GMDN term
Surgical instrument handle, non-torque-limiting
Device class
Class I
Regulation number
884.1690
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 instrument handle, non-torque-limiting

Similar devices in this category

Other devices filed under GYNAECOLOGY AND FERTILITY TREATMENT INSTRUMENTS.

Other devices from Karl Storz SE & CO. KG

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

Properties

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