Jmoon

FDA UDI

Class II (US FDA UDI)

by Shenzhen Ulike Smart Electronics Co., Ltd.

Identity

Trade Name: JMOON FDA UDI
Generic Name: Electrode conductive medium FDA UDI
Model / Reference: 80mL FDA UDI

Identifiers

Primary DI / UDI-DI: 06974667824986 FDA UDI
510(k) Number: K243749 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

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

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

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrode conductive medium

Jmoon by Shenzhen Ulike Smart Electronics Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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INNOVO — Atlantic Therapeutics, Ltd. · Class II
Medline — MEDLINE INDUSTRIES, INC. · Class II
AUVON — Shenzhen Yuwen E-Commerce Co., Ltd. · Class II
Pharmaceutical Innovations — Pharmaceutical Innovations, Inc. · Class II
QUELL — NEUROMETRIX, INC. · Class II

Cleared under the same submission

K243749 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: Shenzhen Ulike Smart Electronics Co., Ltd.

Sources (1)

FDA UDI 35da9604-ea8b-4aae-a05d-ed5b0e65d94f 33 fields · synced May 29, 2026