AeroWrap™ Full Leg

Basic Information

• Brand Name: AeroWrap™ Full Leg
• Primary DI: 00850051939701
• Version / Model: FL-FR-SR-L-SF-L
• Catalog Number: FL-FR-SR-L-SF-L
• Company Name: SUN SCIENTIFIC, INC.
• Labeler DUNS: 609397224
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2024-12-05
• Public Version: 1
• Public Version Date: 2024-12-13
• Public Version Status: New
• Public Device Record Key: 3bffcb67-1ea9-4846-b11a-7aa8dc9be3b5
• Distribution End Date: 2030-10-31

Device Description

The AeroWrap ™ Full Leg System is comprised of inflatable gradient compression sleeves, a Brace sleeve from the ankle to the knee a Thigh sleeve from the knee to the crotch, a compression knee wrap, and a foot compression wrap. A hand pump is included to provide static compression for compression therapy. The AeroWrap™ Full Leg gradient compression system sleeves are non-sterile single patient use medical devices. An inflation source can be attached to the inflation valve on the sleeve. There is a hand pump provided as an inflation source to provide static compression. The systems are intended for hospital and outpatient use..

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: Yes
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: Yes
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
MHW	Dressing, Compression	General Hospital	880.5075	1

GMDN Terms

Code	Name	Definition	Implantable	Status
44762	Multi-chamber venous compression system garment, single-use	A non-sterile, inflatable device in the form of a stocking, sleeve, or suit intended to be applied to the limbs externally to promote venous blood flow. As part of a compression system, the device applies pressure to the extremities through the sequential inflation of several chambers. The resulting increased venous blood flow may help to treat/prevent oedema, deep vein thrombosis (DVT) and pulmonary embolism (PE) in non-ambulatory patients or patients at risk. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00850051939701	GS1

Customer Contacts

• Phone: [phone]
• Email: [email protected]