Kendall SCD 74043

GUDID 20884521130903

Sequential Compression Comfort Tear-Away Sleeves,Thigh Length, Large

Cardinal Health, Inc.

Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use

• Primary Device ID: 20884521130903
• NIH Device Record Key: 15af37a5-d11d-4e1e-acbc-6f9e6bdd53f5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kendall SCD
• Version Model Number: 74043
• Catalog Number: 74043
• Company DUNS: 080935429
• Company Name: Cardinal Health, Inc.
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884521130906 [Primary]
GS1	20884521130903 [Package]; Contains: 10884521130906; Package: CASE [3 Units]; In Commercial Distribution

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: 7
• Public Version Date: 2019-06-17
• Device Publish Date: 2016-09-24

On-Brand Devices [Kendall SCD]

• 40884521052261: Express Tear-Away Sleeves,Thigh Length, Medium
• 40884521052216: Express Tear-Away Sleeves,Thigh Length, Large
• 40884521052179: Express Tear-Away Sleeves,Thigh Length, Small
• 40884521052131: Express Sleeves,Knee Length, Large
• 40884521052087: Express Sleeves,Knee Length, Medium
• 40884521051684: Express Sleeves,Thigh Length, Large
• 40884521051677: Express Sleeves,Thigh Length, Medium
• 40884521051608: Express Sleeves,Thigh Length, Small
• 40884521021045: Express Sleeves,Thigh Length, Medium
• 40884521021038: Express Sleeves,Knee Length, Medium
• 20884521003146: Express Foot Cuff,Medium
• 10884521021051: True content to be populated as part of rebranding
• 10884521003163: Express Foot Cuff,Large
• 30884521000258: Express Tear-Away Sleeves,Thigh Length, Large
• 10884521528512: Kendall SCD Sequential Compression Comfort Sleeves, Thigh Length, Large
• 10884521528505: Kendall SCD Sequential Compression Comfort Sleeves, Thigh Length, Medium
• 10884521528499: Kendall SCD Sequential Compression Comfort Sleeves, Thigh Length, Small
• 10884521528482: Kendall SCD Sequential Compression Comfort Sleeves, Thigh Length, X-Small
• 20884521130903: Sequential Compression Comfort Tear-Away Sleeves,Thigh Length, Large
• 20884521130897: Sequential Compression Comfort Tear-Away Sleeves, Thigh Length, Medium
• 20884521130880: Sequential Compression Comfort Tear-Away Sleeves Thigh Length, Small
• 20884521130873: Sequential Compression Comfort Sleeves,Knee Length, Large
• 20884521130866: Sequential Compression Comfort Sleeves,Knee Length, Medium
• 20884521130859: Sequential Compression Comfort Sleeves,Knee Length, Small
• 20884521130842: Sequential Compression Comfort Sleeves,Thigh Length, Large
• 20884521130835: Sequential Compression Comfort Sleeves,Thigh Length, Medium
• 20884521130828: Sequential Compression Comfort Sleeves,Thigh Length, Small
• 20884521130811: Sequential Compression Comfort Sleeves,Thigh Length, X-Small
• 10884521138353: Express Sequential Compression System,Vascular Refill Detection
• 10884521138346: Express Sequential Compression System,Vascular Refill Detection
• 10884521100237: Express Sequential Compression System,Vascular Refill Detection
• 10884521100220: Express Sequential Compression System,Vascular Refill Detection
• 10884521100213: Express Sequential Compression System,Vascular Refill Detection
• 10884521100176: Express Sequential Compression System Vascular Refill Detection
• 10884521100169: Express Sequential Compression System,Vascular Refill Detection
• 10884521082755: Express Sequential Compression System,Vascular Refill Detection
• 10884521082632: Express Sequential Compression System,Vascular Refill Detection
• 10884521082625: Express Sequential Compression System,Vascular Refill Detection
• 10884521082618: Express Sequential Compression System,Vascular Refill Detection
• 10884521081840: Express Sequential Compression System,Vascular Refill Detection
• 10884521081826: Express Sequential Compression System,Vascular Refill Detection
• 20884521025179: Express Foot Cuff,Large
• 20884521025162: Express Foot Cuff,Medium
• 20884521007021: Controller Tubing Extension Assembly,3' (91.4 cm)
• 20884521007014: Controller Tubing Assembly,13' (4 m)
• 20884521006994: Controller Tubing Extension Assembly,4' (1.2 m)
• 20884521006956: Controller Tubing Assembly,7' (2.1 m)
• 20884521009001: Express Sleeves,Knee Length, X-Large
• 30884521008834: Express Sleeves,Knee Length, Large
• 30884521008810: Express Sleeves,Thigh Length, Large