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Instrumentation Difra VIDEOSTAR II

by Instrumentation Difra SA

Instrumentation Difra VIDEOSTAR II (22092) is a Class I device made by Instrumentation Difra SA, listed in FDA GUDID since 17 Sep 2018 (UDI-DI B51622092), 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 NumberB51622092 UDI-DI Date17 Sep 2018ListedStatusListed 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  • Withdrawn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
Instrumentation Difra
Generic name
Posturography system platform
Model / Ref / Catalog
VIDEOSTAR II, 22092
Primary DI / UDI-DI
B51622092
FDA product code
HJJ
GMDN term
Posturography system platform
Device class
Class I
Regulation number
886.1390
GUDID distribution status
In Commercial Distribution

Related devices

Category: Posturography system platform

Other devices from S.A. Instrumentation Difra

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Properties

  • Contains latex
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)