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Hem Fs

by Medical Measurement Systems B.V.

Hem Fs is a Class II device made by Medical Measurement Systems B.V., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 08717775955870), 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 Number08717775955870 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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

Generic name
Electromyograph
Model / reference
HEM FS
Primary DI / UDI-DI
08717775955870
FDA product code
FFX
GMDN term
Electromyograph
Device class
Class II
Regulation number
876.1725
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FFX (SYSTEM, GASTROINTESTINAL MOTILITY (ELECTRICAL)).

Other devices from Medical Measurement Systems B.V.

See all devices from Medical Measurement Systems B.V. →

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)