dorsaVi - V6 EMG DAP

FDA UDI

Class II (US FDA UDI)

by Dorsavi Ltd

Identity

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

Identifiers

Catalog Number: RS-A865 FDA UDI
Primary DI / UDI-DI: B758000RDA890 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Psychophysiological biofeedback system

dorsaVi - V6 EMG DAP by Dorsavi Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Psychophysiological biofeedback system.

Axon — EXSURGO LIMITED · Class II
TT-EEG MONO/BIPOLAR ELECTRODE KIT — Thought Technology Ltd. · Class II
DC-EEG TWO CHANNEL CONNECTIVIT KIT — Thought Technology Ltd. · Class II
Switch Sensor Cable — Thought Technology Ltd. · Class II
Flexcomp Infiniti Encoder — Thought Technology Ltd. · Class II
Trigno Avanti Mini Sensor — DELSYS, INC. · Class II
Pathway — PROMETHEUS GROUP OF NEW HAMPSHIRE LIMITED, THE · Class II
FlexiCAP — DEYMED Diagnostic s.r.o. · Class II

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 II	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Dorsavi Ltd

Sources (1)

FDA UDI 89659d6e-5071-45cd-a9b0-340371bff1c5 36 fields · synced Jun 8, 2026