JMOON

GUDID 16974667825027

Shenzhen Ulike Smart Electronics Co., Ltd.

Physical therapy transcutaneous neuromuscular electrical stimulation system

• Primary Device ID: 16974667825027
• NIH Device Record Key: c917a781-6d09-49ab-a55c-e3bcdec14380
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JMOON
• Version Model Number: M30U MW
• Company DUNS: 618646978
• Company Name: Shenzhen Ulike Smart Electronics Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06974667825020 [Primary]
GS1	16974667825027 [Package]; Contains: 06974667825020; Package: [8 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K243393

FDA Product Code

• NFO: Stimulator, Transcutaneous Electrical, Aesthetic Purposes

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-16
• Device Publish Date: 2025-06-07

On-Brand Devices [JMOON]

• 16974667825058: M30U MP
• 16974667825041: M30U SK
• 16974667825034: M30U SG
• 16974667825027: M30U MW
• 16974667825010: M30U PR
• 16974667825003: 30mL
• 16974667824990: 50mL
• 16974667824983: 80mL