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Medi-Stim PREMIER STIM PLUS

by Everyway Medical Instruments Co., Ltd.

Medi-Stim PREMIER STIM PLUS is a Class II device made by Everyway Medical Instruments Co., Ltd., listed in FDA GUDID since 2 Sep 2026 (UDI-DI 04719871183861), 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 Number04719871183861 UDI-DI Date2 Sep 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  • Withdrawn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
Medi-Stim
Generic name
Physical therapy transcutaneous neuromuscular electrical stimulation system
Model / reference
PREMIER STIM PLUS
Primary DI / UDI-DI
04719871183861
FDA product code
NUH, NGX
GMDN term
Physical therapy transcutaneous neuromuscular electrical stimulation system
Device class
Class II
Regulation number
882.5890, 890.5850
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Other devices from Everyway Medical Instruments Co., Ltd.

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Properties

  • Over-the-counter
Other properties (14, all answered No)