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Freeemg 300

by Bts SpA

Freeemg 300 (BTSFE3) is a Class II device made by Bts SpA, listed in FDA GUDID since 6 Jul 2016 (UDI-DI B179FE3), 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 NumberB179FE3 UDI-DI Date6 Jul 2016ListedStatusListed 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  • Withdrawn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
Freeemg
Generic name
Electromyograph
Model / Ref / Catalog
300, BTSFE3
Primary DI / UDI-DI
B179FE3
FDA product code
HCC
GMDN term
Electromyograph
Device class
Class II
Regulation number
882.5050
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HCC (Device, Biofeedback).

Other devices from Bts SpA

  • Smart Dx Evo Hybrid

    Class II
  • Tmjoint 1.0

    Class II
  • Smart Dx EVO2

    Class II
  • P6000

    Class I

See all devices from Bts SpA →

Properties

  • Prescription use
  • Combination product
  • Premarket exempt
  • Serial number
Other properties (11, all answered No)