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Movement Suite / V5 Sensor Kit 0000VMV50

by Dorsavi Ltd

Movement Suite / V5 Sensor Kit 0000VMV50 is a Class I device made by Dorsavi Ltd, listed in FDA GUDID since 26 Sep 2019 (UDI-DI B7580000VMV50), 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 NumberB7580000VMV50 UDI-DI Date26 Sep 2019ListedStatusListed 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  • Withdrawn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
Movement Suite / V5 Sensor Kit
Generic name
Psychophysiological biofeedback system
Model / Ref / Catalog
0000VMV50, VMV50
Primary DI / UDI-DI
B7580000VMV50
FDA product code
KQX, HCC, IKN
GMDN term
Psychophysiological biofeedback system
Device class
Class I
Regulation number
888.1500, 882.5050, 890.1375
GUDID distribution status
In Commercial Distribution

Related devices

Category: Psychophysiological biofeedback system

Similar devices in this category

Other devices filed under Psychophysiological biofeedback system.

Other devices from Dorsavi Ltd

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Properties

  • Prescription use
  • Convenience kit
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)