Belifu

GUDID 16973810850435

Shenzhen Jian Feng Electronic Technology Co., Ltd.

Physical therapy transcutaneous neuromuscular electrical stimulation system

• Primary Device ID: 16973810850435
• NIH Device Record Key: c71a99e8-715a-48fa-98d6-70a20c394529
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Belifu
• Version Model Number: SM9126
• Company DUNS: 560082555
• Company Name: Shenzhen Jian Feng Electronic Technology 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: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06973810850438 [Primary]
GS1	16973810850435 [Package]; Contains: 06973810850438; Package: [60 Units]; In Commercial Distribution
GS1	26973810850432 [Package]; Contains: 06973810850438; Package: [40 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K223825

FDA Product Code

• NGX: Stimulator, Muscle, Powered, For Muscle Conditioning

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: 2026-02-06
• Device Publish Date: 2026-01-29

On-Brand Devices [Belifu]

• 06973810850032: FM-B2403
• 16973810850435: SM9126