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Eagle Electrode Manufacturing Self Adhering Electrodes

FDA UDI

Class II (US FDA UDI)

by Eagle Electrode Manufacturing, Llc

Identity

Trade Name
Eagle Electrode Manufacturing Self Adhering Electrodes FDA UDI
Generic Name
Transcutaneous electrical stimulation electrode, single-use FDA UDI
Device Name
2 inch round electrodes for use with TENS, NMES, IFC, EMG devices FDA UDI
Model / Reference
EEM2RND FDA UDI
Description
2 inch round electrodes for use with TENS, NMES, IFC, EMG devices FDA UDI

Identifiers

Catalog Number
EEM2RND FDA UDI
Primary DI / UDI-DI
00867991000217 FDA UDI
510(k) Number
K030800 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Transcutaneous electrical stimulation 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

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Transcutaneous electrical stimulation electrode, single-use

Eagle Electrode Manufacturing Self Adhering Electrodes by Eagle Electrode Manufacturing, Llc — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Transcutaneous electrical stimulation electrode, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3203f607-0764-4da4-9e6f-2b458d7f3685 36 fields · synced Jun 6, 2026