PowerDot

GUDID 00810036059619

Theragun, Inc

Transcutaneous electrical stimulation electrode, single-use

• Primary Device ID: 00810036059619
• NIH Device Record Key: 3e4be5ef-e406-4e40-b4c6-c9d3253c317d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PowerDot
• Version Model Number: PD Blue Magnetic Pad- Butterfly
• Company DUNS: 080550811
• Company Name: Theragun, Inc
• 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: 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	00810036059619 [Primary]

FDA Product Code

• GXY: Electrode, Cutaneous

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: 2022-04-26
• Device Publish Date: 2022-04-18

On-Brand Devices [PowerDot ]

• 00840295400105: PowerDot PD-01M2
• 00810036059619: PD Blue Magnetic Pad- Butterfly
• 00810036056175: PowerDot PD-01M2
• 00810036056168: PowerDot PD-01M2
• 00810036056151: PD Blue Magnetic Pad