DR-HO'S

GUDID 06970742221497

Neck Comforter This product is used for the peripheral fixation of the neck and the longitudinal traction of the cervical vertebra.It is composed by cloth sleeves, three TPU round air bags and inflatable balls.It is mainly through stretching the cervical interspace under the inflatable state, reducing the pressure of the cervical interspace, improving the burden of the ligaments around the cervical vertebra, so that the injured cervical vertebra can get a full rest.

Guangzhou Xinbo Electronic Co., Ltd.

Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device Wearable cervical spine traction device

• Primary Device ID: 06970742221497
• NIH Device Record Key: 021a3228-5854-4a26-bdf2-4e99323fa820
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DR-HO'S
• Version Model Number: XB-JT1000
• Company DUNS: 530683813
• Company Name: Guangzhou Xinbo Electronic 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: true
• Serial Number: false
• Manufacturing Date: false
• 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	06970742221497 [Primary]

FDA Product Code

• KQZ: Component, Traction, Non-Invasive

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: 2020-03-09
• Device Publish Date: 2020-03-01