Hose

GUDID 18809802640679

Single Hose 2m 1ea [One polybag]

DAESUNG MAREF CO.,LTD.

Intermittent venous compression system

• Primary Device ID: 18809802640679
• NIH Device Record Key: e7a25d55-11e4-4216-afb9-42a940a3b8c6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hose
• Version Model Number: 1000370
• 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: 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: true
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	08809802640672 [Primary]
GS1	18809802640679 [Package]; Contains: 08809802640672; Package: Box [10 Units]; In Commercial Distribution
GS1	28809802640676 [Package]; Contains: 08809802640672; Package: Box [20 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K202395

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: 2021-12-27
• Device Publish Date: 2021-12-17

On-Brand Devices [Hose]

• 18809802640709: Single Hose 1.5m 1ea [One polybag]
• 18809802640693: DISTRIBUTION TUBING 0.5m 1ea [One polybag]
• 18809802640686: Double Hose 2m (including foot acupressure) 1ea [One polybag]
• 18809802640679: Single Hose 2m 1ea [One polybag]