Auvon

FDA UDI

Class II (US FDA UDI)

by Shenzhen Yuwen E-Commerce Co., Ltd.

Identity

Trade Name: AUVON FDA UDI
Generic Name: Electrode conductive medium FDA UDI
Device Name: Intended for use with electric stimulation therapy devices, such as TENS and EMS. Conductive Gel is used with external electrodes to reduce the impedance of the contact between the electrode and the skin. FDA UDI
Model / Reference: CG2252 FDA UDI
Description: Intended for use with electric stimulation therapy devices, such as TENS and EMS. Conductive Gel is used with external electrodes to reduce the impedance of the contact between the electrode and the skin. FDA UDI

Identifiers

Primary DI / UDI-DI: 16971292006746 FDA UDI
FDA Product Code: GYB FDA UDI
GMDN Term: Electrode conductive medium FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.1275 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

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Electrode conductive medium

Auvon by Shenzhen Yuwen E-Commerce 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: Shenzhen Yuwen E-Commerce Co., Ltd.

Sources (1)

FDA UDI 29de6a51-75c5-4059-b144-cf6a045d80dc 34 fields · synced May 30, 2026