Belifu

GUDID 06973810850032

Shenzhen Jian Feng Electronic Technology Co., Ltd.

Physical therapy transcutaneous neuromuscular electrical stimulation system

• Primary Device ID: 06973810850032
• NIH Device Record Key: e5d420c8-1f1b-4726-811f-6b557c79d2d0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Belifu
• Version Model Number: FM-B2403
• Company DUNS: 560082555
• Company Name: Shenzhen Jian Feng Electronic Technology Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• 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	06973810850032 [Primary]
GS1	16973810850039 [Package]; Package: [45 Units]; In Commercial Distribution

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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2021-02-19
• Device Publish Date: 2020-11-03

Devices Manufactured by Shenzhen Jian Feng Electronic Technology Co., Ltd.

• 16973810850404 - AVCOO: 2024-12-23
• 16973810850398 - AUVON: 2024-11-11
• 16973810850374 - No: 2024-09-12
• 16973810850350 - No: 2024-08-29
• 16973810850367 - No: 2024-08-29
• 16973810850343 - No: 2024-08-21
• 06973810850339 - Na: 2024-08-16
• 16973810850312 - No: 2024-07-24