RecoveryAir

GUDID 00810036057035

Powered inflatable tube massager

Theragun, Inc

Multi-chamber venous compression system garment, reusable

• Primary Device ID: 00810036057035
• NIH Device Record Key: 950872e9-b635-4b39-8701-f57cfacb3552
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RecoveryAir
• Version Model Number: RecoveryAir PRO Pump
• 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	00810036057035 [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: 2021-12-31
• Device Publish Date: 2021-12-23

On-Brand Devices [RecoveryAir]

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• 00810036057035: Powered inflatable tube massager
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• 00810036056229: Powered inflatable tube massager