DVT-4000S

GUDID 18809315675656

Main device 1ea, Tubing(3m) 2ea [One set box]

DAESUNG MAREF CO.,LTD.

Sequential venous compression system inflator

• Primary Device ID: 18809315675656
• NIH Device Record Key: e8a17427-34ae-4fcf-9f1a-bf2d888c0099
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DVT-4000S
• Version Model Number: DVT4200-3
• 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: true
• 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	08809315675659 [Primary]
GS1	18809315675656 [Package]; Contains: 08809315675659; Package: Box [2 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K203417

FDA Product Code

• JOW: Sleeve, Limb, Compressible

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-09-19
• Device Publish Date: 2021-04-09

On-Brand Devices [DVT-4000S]

• 18809315675663: Main Device 1ea, Tubing(Single hose 1.5m) 2ea [One set box]
• 08809315675314: DVT-4000S Device 1ea
• 18809315675656: Main device 1ea, Tubing(3m) 2ea [One set box]
• 18809315675649: Main device 1ea, Tubing (2.3m) 2ea [One set box]