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Lccs Ikd-Kd-30-Lc

by Lccs Products Limited

Lccs Ikd-Kd-30-Lc is a Class II device made by Lccs Products Limited, listed in FDA GUDID since 4 Aug 2026 (UDI-DI 04895233605667), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04895233605667 UDI-DI Date4 Aug 2026ListedStatusListed 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  • Withdrawn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
Lccs
Generic name
Electrical-only medical device connection cable, reusable
Model / reference
IKD-KD-30-LC
Description
Electrode Adapt Cable
Primary DI / UDI-DI
04895233605667
FDA product code
IKD
GMDN term
Electrical-only medical device connection cable, reusable
Device class
Class II
Regulation number
890.1175
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code IKD (Cable, Electrode).

Other devices from Lccs Products Limited

See all devices from Lccs Products Limited →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)