TheraFace

GUDID 00810036056809

Theragun, Inc

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• Primary Device ID: 00810036056809
• NIH Device Record Key: cbe8a0e2-5b24-4a0b-81b4-548f1488b245
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TheraFace
• Version Model Number: TheraFace Hot & Cold Rings White
• Company DUNS: 080550811
• Company Name: Theragun, Inc
• 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: true
• 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	00810036056809 [Primary]

FDA Product Code

• IME: Pack, Hot Or Cold, Reusable

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: 2022-01-26
• Device Publish Date: 2022-01-18

On-Brand Devices [TheraFace]

• 00810036056809: TheraFace Hot & Cold Rings White
• 00810036056762: TheraFace Hot & Cold Rings Black
• 00810036056724: The TheraFace PRO is a 4-in-1 handheld device that takes facial wellness to the next level by he
• 00810036056687: The TheraFace PRO is a 4-in-1 handheld device that takes facial wellness to the next level by he