Alpha-Stim Earclip Electrode Pad

FDA UDI

Class III (US FDA UDI)

by Electromedical Products International, Inc.

Identity

Trade Name: Alpha-Stim Earclip Electrode Pad FDA UDI
Generic Name: Electrical probe/electrode conductive pad FDA UDI
Device Name: Alpha-Stim Earclip Electrode Pad FDA UDI
Model / Reference: EEP FDA UDI
Description: Alpha-Stim Earclip Electrode Pad FDA UDI

Identifiers

Primary DI / UDI-DI: 00857869005031 FDA UDI
FDA Product Code: JXK FDA UDI
GMDN Term: Electrical probe/electrode conductive pad FDA UDI

Classification

Device Class: Class III FDA UDI
Regulation Number: 882.5800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Electrical probe/electrode conductive pad

Alpha-Stim Earclip Electrode Pad by Electromedical Products International, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Electrical probe/electrode conductive pad.

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Everyway — EVERYWAY MEDICAL INSTRUMENTS CO., LTD. · Class II
Jiajian — Wuxi Jiajian Medical Instrument Co., Ltd. · Class II
CHATTANOOGA — DJO, LLC · Class I
Home Care — Home Care Technology Co., Ltd. · Class II
TruDenta Earclip Electrode Pad — Electromedical Products International, Inc. · Class III

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class III	Pending data

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Manufacturer

Manufacturer: Electromedical Products International, Inc.

Sources (1)

FDA UDI c6fbb0e2-ea67-42d6-a386-7380f2dc39db 33 fields · synced May 30, 2026