FDA UDI In Commercial Distribution 🇺🇸 United States

AirLife™

DI: 10889483606124 · Model: T260 · AIRLIFE
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
AirLife™
Primary DI
10889483606124
Version / Model
T260
Catalog Number
T260
Company Name
AIRLIFE
Labeler DUNS
119058668
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-07
Public Version
2
Public Version Date
2025-04-17
Public Version Status
Update
Public Device Record Key
f01d249c-4f84-457f-a552-6c578dca2dbe

Device Description

AirLife™ Tri-Flo™ Suction Catheter

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
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
BSY Catheters, Suction, Tracheobronchial

GMDN Terms

Code Name
34041 Tracheobronchial suction/insufflation catheter, single-lumen

Identifiers

Type ID
Package 30889483606128
Primary 10889483606124

Customer Contacts