Syrebo BXB

GUDID 06973408900019

The product is suitable for patients with certain hand movement ability, which can improve the precise control ability of the hand through assisting the hand to realize different gestures and movements. In addition, it can be applied in various training modes such as passive training, mirror training, active training, resistance training, power-assisted training and voice control training, to stimulate and intervene patients' central and peripheral nerves, which is helpful to the recovery of hand movement function of patients.

Shanghai SiYi Intelligent Technology Co., Ltd.

Hand/wrist continuous passive motion exerciser Hand/wrist continuous passive motion exerciser Hand/wrist continuous passive motion exerciser Hand/wrist continuous passive motion exerciser Hand/wrist continuous passive motion exerciser Hand/wrist continuous passive motion exerciser Hand/wrist continuous passive motion exerciser Hand/wrist continuous passive motion exerciser Hand/wrist continuous passive motion exerciser Hand/wrist continuous passive motion exerciser Hand/wrist continuous passive motion exerciser Hand/wrist continuous passive motion exerciser Hand/wrist continuous passive motion exerciser Hand/wrist continuous passive motion exerciser Hand/wrist continuous passive motion exerciser Hand/wrist continuous passive motion exerciser

• Primary Device ID: 06973408900019
• NIH Device Record Key: 3288eaec-36bd-4599-ba16-1ff514d24ab7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Syrebo
• Version Model Number: SY-HR
• Catalog Number: BXB
• Company DUNS: 416757473
• Company Name: Shanghai SiYi Intelligent Technology Co., Ltd.
• 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: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• 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	06973408900019 [Primary]

FDA Product Code

• BXB: Exerciser, Powered

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: 2021-06-01
• Device Publish Date: 2021-05-24