VU

GUDID 06971234479501

Air Pressure Therapy System

Xiamen Weiyou Intelligent Technology Co.,Ltd

Large-area electric massager Large-area electric massager Large-area electric massager Large-area electric massager Large-area electric massager Large-area electric massager Large-area electric massager Large-area electric massager Large-area electric massager Large-area electric massager Large-area electric massager Large-area electric massager Large-area electric massager Large-area electric massager Large-area electric massager Large-area electric massager Freestanding electric massager Freestanding electric massager Freestanding electric massager Freestanding electric massager Freestanding electric massager Freestanding electric massager Freestanding electric massager Freestanding electric massager Freestanding electric massager Freestanding electric massager Freestanding electric massager Freestanding electric massager Freestanding electric massager Freestanding electric massager Freestanding electric massager Freestanding electric massager

• Primary Device ID: 06971234479501
• NIH Device Record Key: 59604b70-33db-40b9-84b3-6f3db9f56bd3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VU
• Version Model Number: VU-IPC12
• Company DUNS: 549592185
• Company Name: Xiamen Weiyou Intelligent 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: false
• Serial Number: true
• Manufacturing Date: true
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06971234479501 [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: 2021-12-07
• Device Publish Date: 2021-11-29

On-Brand Devices [VU]

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• 06971234479242: Air Pressure Therapy System
• 06971234479648: Headache physiotherapy device
• 06971234479631: electric muscle stimulation
• 06971234479624: hand rehabilitation robot
• 06971234479617: hand rehabilitation robot
• 06971234479594: hand rehabilitation robot
• 06971234479587: hand rehabilitation robot
• 06971234479570: hand rehabilitation robot
• 06971234479549: Air Pressure Therapy System
• 06971234479532: Air Pressure Therapy System
• 06971234479525: Air Pressure Therapy System
• 06971234479518: Air Pressure Therapy System
• 06971234479501: Air Pressure Therapy System
• 06971234479495: Air Pressure Therapy System
• 06971234479488: Air Pressure Therapy System
• 06971234479471: Air Pressure Therapy System
• 06971234479464: Air Pressure Therapy System
• 06971234479440: Air Pressure Therapy System
• 06971234479433: Air Pressure Therapy System
• 06971234479426: Air Pressure Therapy System
• 06971234479419: Air Pressure Therapy System
• 06971234479402: Air Pressure Therapy System
• 06971234479396: Air Pressure Therapy System
• 06971234479372: Air Pressure Therapy System
• 06971234479358: Air Pressure Therapy System
• 06971234479341: Air Pressure Therapy System
• 06971234479334: Air Pressure Therapy System
• 06971234479327: Air Pressure Therapy System
• 06971234479303: Air Pressure Therapy System
• 06971234479297: Air Pressure Therapy System
• 06971234479280: Air Pressure Therapy System
• 06971234479273: Air Pressure Therapy System
• 06971234479266: Air Pressure Therapy System
• 06971234479655: Medical parallel transport bed