DVT-2600

GUDID 08809802646803

Main Device 1ea

DAESUNG MAREF CO.,LTD.

Sequential venous compression system

• Primary Device ID: 08809802646803
• NIH Device Record Key: e7c1d25e-30ec-4656-ab4d-24c2ceeffc87
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DVT-2600
• Version Model Number: DVT3120
• Company DUNS: 688817949
• Company Name: DAESUNG MAREF 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08809802646803 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K203016

FDA Product Code

• JOW: Sleeve, Limb, Compressible

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: 2025-12-29
• Device Publish Date: 2025-12-19

On-Brand Devices [DVT-2600]

• 18809315675434: Main device 1ea, Tubing(Single hose 3m) 2ea, [One set]
• 18809315675427: Main device 1ea, Tubing(Single hose 2.3m) 2ea [One set]
• 08809315675307: DVT-2600 Device 1ea
• 18809802646817: Main Device 1ea, Tubing(2.3m) 2ea [One Set Box]
• 08809802646803: Main Device 1ea