VONMIE

GUDID 06973209160049

TENS and PMS Feet Pad

Shenzhen Leading Perfectin Technology Co.,Ltd

Transcutaneous electrical stimulation electrode, single-use

• Primary Device ID: 06973209160049
• NIH Device Record Key: f0f55163-3c84-4897-b0a3-b0bbb3a772dc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VONMIE
• Version Model Number: S3
• Company DUNS: 554459050
• Company Name: Shenzhen Leading Perfectin 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: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: true
• 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	06973209160049 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K183674

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: 3
• Public Version Date: 2021-02-19
• Device Publish Date: 2020-06-01

On-Brand Devices [VONMIE]

• 06973209160056: TENS and PMS Hips Pad
• 06973209160049: TENS and PMS Feet Pad
• 06973209160032: TENS and PMS Abdomen Pad
• 06973209160025: TENS and PMS Arms and Legs Pad