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NeuroPlus™

FDA UDI

Class II (US FDA UDI)

by Graphic Controls Acquisition Corp

Identity

Trade Name
NeuroPlus™ FDA UDI
Generic Name
Analytical non-scalp cutaneous electrode FDA UDI
Device Name
Disposable Medical Electrodes 60 per pouch, 10 pouch per case 600 per case FDA UDI
Model / Reference
A10040-60 FDA UDI
Description
Disposable Medical Electrodes 60 per pouch, 10 pouch per case 600 per case FDA UDI

Identifiers

Catalog Number
A10040-60 FDA UDI
Primary DI / UDI-DI
60813150020864 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

NeuroPlus™ 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 2aec51af-2710-47a1-bdc3-9208dbbed915 35 fields · synced Jun 8, 2026