SP-1000

GUDID 18809802645315

Main Device 1ea, Leg Sleeve (XL) 2ea, Double Tubing 1ea [One Set Box]

DAESUNG MAREF CO.,LTD.

Sequential venous compression system inflator

• Primary Device ID: 18809802645315
• NIH Device Record Key: 5f0ba6e5-965f-4e5e-9cba-2ad15a94152a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SP-1000
• Version Model Number: SP10100-LX
• 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: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	08809802645318 [Primary]
GS1	18809802645315 [Package]; Contains: 08809802645318; Package: Box [2 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: 2025-12-29
• Device Publish Date: 2025-12-19

On-Brand Devices [SP-1000]

• 18809315672020: Main device 1ea, LEG SLEEVE XXLarge 2ea, ARM SLEEVE 1ea, Single Hose 1ea, Double Hose 1ea [One s
• 18809315672013: Main device 1ea, LEG SLEEVE XLarge 2ea, ARM SLEEVE 1ea, Single Hose 1ea, Double Hose 1ea [One se
• 18809315672006: Main device 1ea, LEG SLEEVE Large 2ea, ARM SLEEVE 1ea, Single Hose 1ea, Double Hose 1ea [One set
• 18809315671993: Main device 1ea, ARM SLEEVE 1ea, Single Hose 1ea, Double Hose 1ea [One set box]
• 18809315671986: Main device 1ea, CENTER BODY SLEEVE 1ea, CENTER BODY EXTENSION ZIPPER 2ea, Double Hose 1ea [One
• 18809315671917: Main device 1ea, LEG SLEEVE XXLarge 2ea, Single Hose 1ea, Double Hose 1ea [One set box]
• 18809315671900: Main device 1ea, LEG SLEEVE XLarge 2ea, Single Hose 1ea, Double Hose 1ea [One set box]
• 18809315671894: Main device 1ea, LEG SLEEVE Large 2ea, Single Hose 1ea, Double Hose 1ea [One set box]
• 18809315671887: Main device 1ea, LEG SLEEVE XXLarge 2ea, Double Hose 1ea [One set box]
• 18809315671870: Main device 1ea, LEG SLEEVE XLarge 2ea, Double Hose 1ea [One set box]
• 18809315671863: Main device 1ea, LEG SLEEVE Large 2ea, Double Hose 1ea [One set box]
• 08809315671859: Main device 1ea
• 08809802645356: Main Device 1ea, Leg Sleeve (XXL) 2ea, Double Tubing 1ea, Recovery Bag 1ea [One Set Box]
• 08809802645349: Main Device 1ea, Leg Sleeve (XL) 2ea, Double Tubing 1ea, Recovery Bag 1ea [One Set Box]
• 08809802645332: Main Device 1ea, Leg Sleeve (L) 2ea, Double Tubing 1ea, Recovery Bag 1ea [One Set Box]
• 18809802645322: Main Device 1ea, Leg Sleeve (XXL) 2ea, Double Tubing 1ea [One Set Box]
• 18809802645315: Main Device 1ea, Leg Sleeve (XL) 2ea, Double Tubing 1ea [One Set Box]
• 18809802645308: Main Device 1ea, Leg Sleeve (L) 2ea, Double Tubing 1ea [One Set Box]
• 08809802645295: Main Device 1ea