Therabody

GUDID 00840295405704

Powered inflatable tube massager

Theragun, Inc

Multi-chamber venous compression system garment, reusable

• Primary Device ID: 00840295405704
• NIH Device Record Key: bf2f1c2e-abd2-4887-ad81-e4f2c810ebaa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Therabody
• Version Model Number: JetBoots Prime Medium
• 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: 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	00840295405704 [Primary]

FDA Product Code

• IRP: Massager, Powered Inflatable Tube

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: 2024-07-25
• Device Publish Date: 2024-07-17

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• 00810036058230: RecoveryPulse CALF MEDIUM
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• 00810036057950: RecoveryPulse Arm EXTRA LARGE
• 00810036057912: RecoveryPulse Arm LARGE
• 00810036057875: RecoveryPulse Arm MEDIUM
• 00810036057837: RecoveryPulse Arm SMALL
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