Motion Space

GUDID 06976019120371

Air Compression Leg Massager(Single)

Huizhou XINYI Technology Co., LTD

Pneumatic massager

• Primary Device ID: 06976019120371
• NIH Device Record Key: 502fc3b7-87e8-4eed-be70-bbae0d1448f5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Motion Space
• Version Model Number: YY-A01L
• Company DUNS: 707980076
• Company Name: Huizhou XINYI Technology Co., LTD
• 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: false
• 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	06976019120371 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K240981

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: 2024-10-14
• Device Publish Date: 2024-10-05

On-Brand Devices [Motion Space]

• 06976019120371: Air Compression Leg Massager(Single)
• 06976019120364: Air Compression Leg Massager(Pair)