Utopia Gear

GUDID 00862081000344

MIDWESTERN SOLUTIONS

Transcutaneous electrical stimulation electrode

• Primary Device ID: 00862081000344
• NIH Device Record Key: 8f52317a-cf0f-44b1-9857-bcfaff41e624
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Utopia Gear
• Version Model Number: XL Electrode Pads
• Company DUNS: 048681673
• Company Name: MIDWESTERN SOLUTIONS
• 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: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00862081000344 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K092546

FDA Product Code

• GXY: Electrode, Cutaneous

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: 2018-07-06
• Device Publish Date: 2016-09-27

On-Brand Devices [Utopia Gear]

• 00862081000344: XL Electrode Pads
• 00862081000337: Large Electrode Pads
• 00862081000320: Massage Pro 2.0
• 00862081000313: Massage Pro Mini
• 00862081000306: Massage Pro 3.0
• 00862081000375: Pro 4.0