A-V Impulse 6060

GUDID 10884521100152

6000 Series Controller

Cardinal Health, Inc.

Intermittent venous compression system

• Primary Device ID: 10884521100152
• NIH Device Record Key: f28708d7-b982-46fe-a276-515f96b0a1ac
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: A-V Impulse
• Version Model Number: 6060
• Catalog Number: 6060
• 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: 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

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

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884521100152 [Primary]

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: 2019-04-15
• Device Publish Date: 2016-10-13

On-Brand Devices [A-V Impulse]

• 20884521101453: Tubing Assembly, Unrestricted, Blue
• 10884521078123: Impad Rigid Sole Foot Cover, Large
• 10884521078116: Impad Rigid Sole Foot Cover, Medium
• 10884521077386: Impad Rigid Sole Foot Cover, X- Large
• 10884521077379: Impad Rigid Sole Foot Cover, Large
• 10884521077348: Impad Rigid Sole Foot Cover, Medium
• 10884521077300: Impad Rigid Sole Foot Cover;Small
• 10884521100190: 6000 Series Controller,Refurbished
• 10884521100152: 6000 Series Controller
• 20884521077277: Impad Rigid Sole Foot Cover,Left
• 20884521077260: Impad Rigid Sole Foot Cover,Right
• 10884521043923: 6000 Series Controller