AirLife™ 4023RH

GUDID 10889483581995

Reduced Heparin (Arterial Blood Sampler)

Sunmed Group Holdings, LLC

Arterial blood sampling kit

• Primary Device ID: 10889483581995
• NIH Device Record Key: 24cd027e-a220-44ce-8e6c-b9763d42b779
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AirLife™
• Version Model Number: 4023RH
• Catalog Number: 4023RH
• Company DUNS: 119058668
• Company Name: Sunmed Group Holdings, LLC
• Device Count: 1
• DM Exempt: true
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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(800)433-2797
• Email: info@myairlife.com
• Phone: +1(800)433-2797
• Email: info@myairlife.com
• Phone: +1(800)433-2797
• Email: info@myairlife.com
• Phone: +1(800)433-2797
• Email: info@myairlife.com
• Phone: +1(800)433-2797
• Email: info@myairlife.com
• Phone: +1(800)433-2797
• Email: info@myairlife.com
• Phone: +1(800)433-2797
• Email: info@myairlife.com
• Phone: +1(800)433-2797
• Email: info@myairlife.com
• Phone: +1(800)433-2797
• Email: info@myairlife.com
• Phone: +1(800)433-2797
• Email: info@myairlife.com
• Phone: +1(800)433-2797
• Email: info@myairlife.com
• Phone: +1(800)433-2797
• Email: info@myairlife.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10885403271656 [Previous]
GS1	10889483581995 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K822786

FDA Product Code

• CBT: Arterial blood sampling kit

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-12-20
• Device Publish Date: 2024-12-12

On-Brand Devices [AirLife™]

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• 50190752132618: AirLife™ baby safe flow-inflating resuscitation device 1/2 Liter Bag
• 50190752132601: AirLife™ baby safe flow-inflating resuscitation device 1/2 Liter Bag
• 50190752114119: Adult Manual Resuscitator •Oxygen Reservoir Bag, Adult Mask, CO2Detector
• 50190752114102: Adult Manual Resuscitator • Oxygen Reservoir Bag, Adult Mask
• 10889483581995: Reduced Heparin (Arterial Blood Sampler)