No

GUDID 16973810850183

Shenzhen Jian Feng Electronic Technology Co., Ltd.

Physical therapy transcutaneous neuromuscular electrical stimulation system

• Primary Device ID: 16973810850183
• NIH Device Record Key: d8132b1c-a0ed-46de-be74-fb8c6d8d93ae
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: No
• Version Model Number: AS8019
• 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: 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

Customer Support Contacts

• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	06973810850186 [Primary]
GS1	16973810850183 [Package]; Contains: 06973810850186; Package: [48 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K202866

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: 2024-06-07
• Device Publish Date: 2024-05-30

On-Brand Devices [No]

• 06973810850049: FM-B2404
• 06973810850063: FM-B2406
• 06973810850056: FM-B2405
• 16973810854242: TU3424
• 16973810853245: TUP324
• 06973810850070: FM-B2407
• 06973810850025: FM-B2402
• 16973810851517: FM-B1501A
• 16973810850091: FM-B2409
• 16973810850084: FM-B2403A
• 16973810850244: TU2224
• 16973810850237: TA3224
• 16973810850220: AS9020
• 16973810850213: AS9020
• 16973810850206: AS9020
• 16973810850190: AS9020
• 16973810850183: AS8019
• 16973810850176: AS8016
• 16973810850169: AS8016
• 16973810850145: AS8012C
• 16973810850138: AS8012
• 16973810850121: AS8012
• 16973810850114: AS8012
• 16973810850107: AS8012
• 16973810850152: YK15AB
• 16973810850251: TP2208
• 16973810850275: TU1130
• 16973810850268: AS1080
• 16973810850299: TA2224
• 16973810850282: TA2224
• 16973810850305: TU1130
• 16973810850329: TA2224C
• 16973810850312: FM-B2409
• 16973810850343: TA3224
• 16973810850367: AS8016
• 16973810850350: AS8016
• 16973810850374: AS8019