DR-HO'S

GUDID 06970742221466

Decompression Belt This product is used for external fixation of the waist and longitudinal traction of the lumbar spine.It is composed by traction belt and air pump

Guangzhou Xinbo Electronic Co., Ltd.

Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device Wearable lumbar spine traction device

• Primary Device ID: 06970742221466
• NIH Device Record Key: c13a0cee-7b18-435e-81cb-2f46b564e6a4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DR-HO'S
• Version Model Number: Size A/B
• 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	06970742221466 [Primary]

FDA Product Code

• HST: Apparatus, Traction, Non-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: 2020-03-09
• Device Publish Date: 2020-03-01