Theragun

GUDID 00810036050159

Theragun, Inc

Hand-held electric massager

• Primary Device ID: 00810036050159
• NIH Device Record Key: a4580a2c-e1fa-4af9-888f-ea938e29ede9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Theragun
• Version Model Number: Theragun Prime
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810036050159 [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