Theragun

GUDID 00810036050135

Hand held massager

Theragun, Inc

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• Primary Device ID: 00810036050135
• NIH Device Record Key: c788f077-da38-42e5-a41a-4c798a36d0b4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Theragun
• Version Model Number: Theragun PRO
• 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	00810036050135 [Primary]

FDA Product Code

• ISA: Massager, Therapeutic, Electric

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: 2021-10-07
• Device Publish Date: 2021-09-29

On-Brand Devices [Theragun]

• 00810036055116: Wave Solo
• 00810036054676: Wave Duo
• 00810036051217: Wave Roller
• 00810036050197: Elite White
• 00810036050166: Theragun Mini
• 00810036050159: Theragun Prime
• 00810036050142: Theragun Elite
• 00810036050135: Hand held massager