Knee Compression Wrap Large AWK-300

GUDID 00850051939558

Aero-Wrap™ Knee Compression Wrap is designed to provide therapeutic compression therapy, in the inpatient and outpatient setting, in the treatment of edema and lymphedema of the knee or as part of a wound treatment protocol.

SUN SCIENTIFIC, INC.

Compression/pressure sock/stocking, reusable

• Primary Device ID: 00850051939558
• NIH Device Record Key: 1cd357d4-5541-4858-aa33-50397928a341
• Commercial Distribution Discontinuation: 2030-09-25
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Knee Compression Wrap Large
• Version Model Number: KC7550
• Catalog Number: AWK-300
• Company DUNS: 609397224
• Company Name: SUN SCIENTIFIC, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850051939558 [Primary]

FDA Product Code

• MHW: Dressing, Compression

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: 2024-10-03
• Device Publish Date: 2024-09-25

Devices Manufactured by SUN SCIENTIFIC, INC.

• 00850051939565 - AeroWrap™ Full Leg: 2024-12-13 The AeroWrap ™ Full Leg System is comprised of inflatable gradient compression sleeves, a Brace sleeve from the ankle to the k
• 00850051939572 - AeroWrap™ Full Leg: 2024-12-13 The AeroWrap ™ Full Leg System is comprised of inflatable gradient compression sleeves, a Brace sleeve from the ankle to the k
• 00850051939589 - AeroWrap™ Full Leg: 2024-12-13 The AeroWrap ™ Full Leg System is comprised of inflatable gradient compression sleeves, a Brace sleeve from the ankle to the k
• 00850051939596 - AeroWrap™ Full Leg: 2024-12-13 The AeroWrap ™ Full Leg System is comprised of inflatable gradient compression sleeves, a Brace sleeve from the ankle to the k
• 00850051939602 - AeroWrap™ Full Leg: 2024-12-13 The AeroWrap ™ Full Leg System is comprised of inflatable gradient compression sleeves, a Brace sleeve from the ankle to the k
• 00850051939619 - AeroWrap™ Full Leg: 2024-12-13 The AeroWrap ™ Full Leg System is comprised of inflatable gradient compression sleeves, a Brace sleeve from the ankle to the k
• 00850051939626 - AeroWrap™ Full Leg: 2024-12-13 The AeroWrap ™ Full Leg System is comprised of inflatable gradient compression sleeves, a Brace sleeve from the ankle to the k
• 00850051939640 - AeroWrap™ Full Leg: 2024-12-13 The AeroWrap ™ Full Leg System is comprised of inflatable gradient compression sleeves, a Brace sleeve from the ankle to the k