FDA UDI In Commercial Distribution 🇺🇸 United States

AirLife™

DI: 10889483606155 · Model: T261C · AIRLIFE
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
AirLife™
Primary DI
10889483606155
Version / Model
T261C
Catalog Number
T261C
Company Name
AIRLIFE
Labeler DUNS
119058668
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-02-18
Public Version
2
Public Version Date
2025-04-17
Public Version Status
Update
Public Device Record Key
b61cfa56-9269-477b-93a4-511dfa8d6576

Device Description

AirLife™ Tri-Flo™ Suction Catheter With Control Port

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
No
Sterilization Prior Use
No

Product Codes

Code Name
BSY Catheters, Suction, Tracheobronchial

GMDN Terms

Code Name
10749 Airway suction catheter

Identifiers

Type ID
Package 30889483606159
Primary 10889483606155
Previous 10190752145511

Customer Contacts