Jiajian

FDA UDI

Class II (US FDA UDI)

by Wuxi Jiajian Medical Instrument Co., Ltd.

Identity

Trade Name: Jiajian FDA UDI
Generic Name: Electrical probe/electrode conductive pad FDA UDI
Device Name: Flexible and easy to fit electrode can be applied to every contour of the human body. You can use the electrodes many times because of its reliable long lasting gel. 2 Electrodes in sealed foil pouch. FDA UDI
Model / Reference: 50*50mm FDA UDI
Description: Flexible and easy to fit electrode can be applied to every contour of the human body. You can use the electrodes many times because of its reliable long lasting gel. 2 Electrodes in sealed foil pouch. FDA UDI

Identifiers

Primary DI / UDI-DI: 00810011252301 FDA UDI
510(k) Number: K090198 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

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Electrical probe/electrode conductive pad

Jiajian by Wuxi Jiajian Medical Instrument Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical probe/electrode conductive pad.

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

Cleared under the same submission

K090198 also covers:

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: Wuxi Jiajian Medical Instrument Co., Ltd.

Sources (1)

FDA UDI 9cbf8dad-58c4-4da0-b10a-e7c247fbbbd4 34 fields · synced May 30, 2026