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MVAP Medical Supplies

FDA UDI

Class II (US FDA UDI)

by Graphic Controls Acquisition Corp

Identity

Trade Name
MVAP Medical Supplies FDA UDI
Generic Name
Analytical non-scalp cutaneous electrode FDA UDI
Device Name
Sensing Element with Hydrogel 30 per pouch, 10 pouches per case FDA UDI
Model / Reference
FT002 FDA UDI
Description
Sensing Element with Hydrogel 30 per pouch, 10 pouches per case FDA UDI

Identifiers

Catalog Number
FT002 FDA UDI
Primary DI / UDI-DI
10813150022412 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Analytical non-scalp cutaneous electrode FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1320 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Analytical non-scalp cutaneous electrode

MVAP Medical Supplies by Graphic Controls Acquisition Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analytical non-scalp cutaneous electrode.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7c60031a-e5da-4fc6-a9ac-e3b3fb7bdf5e 35 fields · synced May 31, 2026