AirLife™

Basic Information

• Brand Name: AirLife™
• Primary DI: 10190752152151
• Version / Model: 4695T
• Catalog Number: 4695T
• Company Name: AIRLIFE
• Labeler DUNS: 119058668
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2022-08-22
• Public Version: 3
• Public Version Date: 2025-04-17
• Public Version Status: Update
• Public Device Record Key: 61c385b3-0cab-4da6-a19d-a17642ae8953

Device Description

Tri-Flo™ Suction Cath-N-Glove™ Kit

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: No
• 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: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
OFO	Airway suction kit	Anesthesiology	868.6810	1

GMDN Terms

Code	Name	Definition	Implantable	Status
34041	Tracheobronchial suction/insufflation catheter, single-lumen	A sterile flexible tube designed for periodic tracheal and pharyngeal mucus aspiration and inflation of the lungs with a flow of gas from its distal tip. It consists of a single lumen tube for alternating suction and insufflation. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	50190752152159	GS1	CASE	100	In Commercial Distribution
Primary	10190752152151	GS1

Customer Contacts

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