DR-HOS

GUDID 06970742220339

XJ-F-30

Guangzhou Xinbo Electronic Co., Ltd.

Vibration platform exerciser, stationary

• Primary Device ID: 06970742220339
• NIH Device Record Key: aa9b9361-3a07-48db-9964-9425bd2ba5ee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DR-HOS
• Version Model Number: Motionciser
• Company DUNS: 530683813
• Company Name: Guangzhou Xinbo Electronic Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• 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	06970742220339 [Primary]

FDA Product Code

• ISA: Massager, Therapeutic, Electric

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: 2025-07-08
• Device Publish Date: 2025-06-30

On-Brand Devices [DR-HOS]

• 06970742220315: Adjustable Pillow – Leg
• 06970742220308: Adjustable Pillow – Travel size
• 06970742220292: Adjustable Pillow – Children size
• 06970742220285: Adjustable Pillow – Queen size
• 06970742220278: Adjustable Pillow – King size
• 06970742220339: XJ-F-30