← Back to catalogue

Precision Gold

FDA UDI

Class II (US FDA UDI)

by Dymedix Diagnostics, Inc.

Identity

Trade Name
Precision Gold FDA UDI
Generic Name
Analytical scalp electrode, single-use FDA UDI
Device Name
Disposable Gold 9mm Cup EEG Electrode, 80" (2m), 15 pack FDA UDI
Model / Reference
13-10100-8015 FDA UDI
Description
Disposable Gold 9mm Cup EEG Electrode, 80" (2m), 15 pack FDA UDI

Identifiers

Primary DI / UDI-DI
00817377023194 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Analytical scalp electrode, single-use 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Analytical scalp electrode, single-use

Precision Gold by Dymedix Diagnostics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analytical scalp electrode, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI 0f7dab49-bc67-4573-99f0-658d944a8a7a 33 fields · synced May 30, 2026