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dorsaVi

FDA UDI

Class II (US FDA UDI)

by Dorsavi Ltd

Identity

Trade Name
dorsaVi FDA UDI
Generic Name
Psychophysiological biofeedback system FDA UDI
Device Name
Single use disposable application pad adhesive for use with dorsaVi Version 6 Sensors. FDA UDI
Model / Reference
V6 Sensor Adhesive FDA UDI
Description
Single use disposable application pad adhesive for use with dorsaVi Version 6 Sensors. FDA UDI

Identifiers

Catalog Number
RS-A482 FDA UDI
Primary DI / UDI-DI
B758000RDA482 FDA UDI
FDA Product Code
HCC FDA UDI
GMDN Term
Psychophysiological biofeedback system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Psychophysiological biofeedback system

dorsaVi by Dorsavi Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Psychophysiological biofeedback system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dorsavi Ltd

Sources (1)

  • FDA UDI 5fa7d6c6-f616-47b7-9099-b3055b61b35d 36 fields · synced May 30, 2026