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BioScan

FDA UDI

Class II (US FDA UDI)

by International Health Tech

Identity

Trade Name
BioScan FDA UDI
Generic Name
Skin electrical conductance meter FDA UDI
Device Name
Galvanic skin response measurement device. FDA UDI
Model / Reference
MSAS Vantage FDA UDI
Description
Galvanic skin response measurement device. FDA UDI

Identifiers

Primary DI / UDI-DI
00862719000302 FDA UDI
FDA Product Code
GZO FDA UDI
GMDN Term
Skin electrical conductance meter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Depth — 13.25 Inch FDA UDI
Width — 13.5 Inch FDA UDI
Height — 3.125 Inch FDA UDI

Category: Skin electrical conductance meter

BioScan by International Health Tech — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin electrical conductance meter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d5a4b7af-3fc6-43e7-8b80-4186242c674c 35 fields · synced May 31, 2026