Movement Suite / V5 Sensor Kit

FDA UDI

Class I (US FDA UDI)

by Dorsavi Ltd

Identity

Trade Name: Movement Suite / V5 Sensor Kit FDA UDI
Generic Name: Psychophysiological biofeedback system FDA UDI
Device Name: Movement Suite is a wireless medical device that measures, records, and reports movements and muscle activity of the lower back / lumbar spine. The system also measures range of motion in the sagittal and coronal anatomical planes. FDA UDI
Model / Reference: 0000VMV50 FDA UDI
Description: Movement Suite is a wireless medical device that measures, records, and reports movements and muscle activity of the lower back / lumbar spine. The system also measures range of motion in the sagittal and coronal anatomical planes. FDA UDI

Identifiers

Catalog Number: VMV50 FDA UDI
Primary DI / UDI-DI: B7580000VMV50 FDA UDI
FDA Product Code: KQX FDA UDI
HCC FDA UDI
IKN FDA UDI
GMDN Term: Psychophysiological biofeedback system FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.1500 FDA UDI
882.5050 FDA UDI
890.1375 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Psychophysiological biofeedback system

Movement Suite / V5 Sensor Kit by Dorsavi Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Dorsavi Ltd

Sources (1)

FDA UDI aa585df9-f1cc-41f5-8343-8c54ce3dcf37 35 fields · synced Jun 8, 2026