Skip to content

Apk LQB10-LP0

by Apk Technology

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

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

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06946725504369 UDI-DI Date26 Sep 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Apk
Generic name
Electrocardiographic lead set, reusable
Model / reference
LQB10-LP0
Primary DI / UDI-DI
06946725504369
FDA product code
IKD
GMDN term
Electrocardiographic lead set, reusable
Device class
Class II
Regulation number
890.1175
GUDID distribution status
In Commercial Distribution

Other devices from Apk Technology

See all devices from Apk Technology →

Properties

  • Premarket exempt
  • Serial number
  • Expiration date
  • Manufacturing date

Other properties (11)

  • Supplied sterile: No
  • Sterilise before use: No
  • Single use: No
  • Implantable: No
  • Contains latex: No
  • Prescription use: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Lot / batch number: No