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Clickline 49310KT

by Karl Storz SE & CO. KG

Clickline 49310KT is a Class II device made by Karl Storz SE & CO. KG, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04048551168158), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04048551168158 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Clickline
Generic name
Dissection forceps
Model / reference
49310KT
Primary DI / UDI-DI
04048551168158
FDA product code
LQR
GMDN term
Dissection forceps
Device class
Class II
Regulation number
876.5010
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dissection forceps

Other devices from Karl Storz SE & CO. KG

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Properties

  • Sterilise before use
  • Prescription use
Other properties (13, all answered No)