Homedics

GUDID 00031262116666

Modulair compression system universal battery

Huizhou XINYI Technology Co., LTD

Pneumatic massager

• Primary Device ID: 00031262116666
• NIH Device Record Key: 3652ea9c-405d-4ec0-a0ea-62ab7886aabe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Homedics
• Version Model Number: SR-CMX10JA
• Company DUNS: 707980076
• Company Name: Huizhou XINYI 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: true
• Serial Number: false
• Manufacturing Date: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00031262116666 [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: 2025-01-08
• Device Publish Date: 2024-12-31

On-Brand Devices [Homedics]

• 00031262109507: Modulair compression system knee wrap
• 00031262116666: Modulair compression system universal battery
• 00031262116697: Modulair compression system Knee wrap
• 00031262116291: Modulair compression knee foot massager