Compression Therapy Device

GUDID 06971410780100

Guangzhou Longest Science & Technology Co., Ltd.

Intermittent venous compression system

• Primary Device ID: 06971410780100
• NIH Device Record Key: 9412c4ce-550f-4e5f-8cc9-3e3ebb7195fc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Compression Therapy Device
• Version Model Number: LGT-2200SP
• Company DUNS: 527141843
• Company Name: Guangzhou Longest Science & 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: false
• Serial Number: true
• 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	06971410780100 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K191862

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: 2019-11-11
• Device Publish Date: 2019-11-03

On-Brand Devices [Compression Therapy Device]

• 06971410780100: LGT-2200SP
• 06971410780254: LGT-2201DVT