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Dual EMG Electrodes

FDA UDI

Class II (US FDA UDI)

by Noraxon USA, Inc.

Identity

Trade Name
Dual EMG Electrodes FDA UDI
Generic Name
Kinesiology/electromyographic sensor set FDA UDI
Device Name
Wet Ag/AgCl Gel Dual EMG Electrodes 8 pieces per pouch FDA UDI
Model / Reference
272 FDA UDI
Description
Wet Ag/AgCl Gel Dual EMG Electrodes 8 pieces per pouch FDA UDI

Identifiers

Catalog Number
272 FDA UDI
Primary DI / UDI-DI
00816271020315 FDA UDI
FDA Product Code
HCC FDA UDI
GMDN Term
Kinesiology/electromyographic sensor set 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

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Kinesiology/electromyographic sensor set

Dual EMG Electrodes by Noraxon USA, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Kinesiology/electromyographic sensor set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Noraxon USA, Inc.

Sources (1)

  • FDA UDI f672f510-2ee8-4399-a046-5ad85c9bc8ff 35 fields · synced May 30, 2026