Everyway

FDA UDI

Class II (US FDA UDI)

by Everyway Medical Instruments Co., Ltd.

Identity

Trade Name: Everyway FDA UDI
Generic Name: Electrical probe/electrode conductive pad FDA UDI
Device Name: Electrode conductive pad A small, non-sterile device designed to facilitate electrical conduction between an electrical stimulation electrode and the skin. It is typically contoured to fit on a particular type of electrode and is made of an absorbent material (e.g., felt) that may be soaked in a conduction fluid. FDA UDI
Model / Reference: TKF5050 FDA UDI
Description: Electrode conductive pad A small, non-sterile device designed to facilitate electrical conduction between an electrical stimulation electrode and the skin. It is typically contoured to fit on a particular type of electrode and is made of an absorbent material (e.g., felt) that may be soaked in a conduction fluid. FDA UDI

Identifiers

Primary DI / UDI-DI: 04719871183489 FDA UDI
FDA Product Code: GXY FDA UDI
GMDN Term: Electrical probe/electrode conductive pad 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

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MRI Safety

MR Safe FDA UDI

Category: Electrical probe/electrode conductive pad

Everyway by Everyway Medical Instruments Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 II	Pending data

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Manufacturer

Manufacturer: Everyway Medical Instruments Co., Ltd.

Sources (1)

FDA UDI 0fed4617-ff3d-44cd-9550-76174f151780 33 fields · synced Jun 1, 2026