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Everyway TKF50100V

by Everyway Medical Instruments Co., Ltd. 2 variants

Everyway TKF50100V is a Class II device made by Everyway Medical Instruments Co., Ltd., listed in FDA GUDID since 17 Mar 2022 (UDI-DI 04719871184875), 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 Number04719871184875 UDI-DI Date17 Mar 2022ListedStatusListed 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  • Withdrawn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
Everyway
Generic name
Transcutaneous electrical stimulation electrode, reusable
Model / reference
TKF50100V
Primary DI / UDI-DI
04719871184875
FDA product code
GXY
GMDN term
Transcutaneous electrical stimulation electrode, reusable
Device class
Class II
Regulation number
882.1320
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Related devices

Category: Transcutaneous electrical stimulation electrode, reusable

Other devices from Everyway Medical Instruments Co., Ltd.

See all devices from Everyway Medical Instruments Co., Ltd. →

Properties

  • Over-the-counter
  • Serial number
Other properties (13, all answered No)