FDA UDI In Commercial Distribution 🇺🇸 United States

AirLife™

DI: 10889483606254 · Model: T62 · AIRLIFE
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
AirLife™
Primary DI
10889483606254
Version / Model
T62
Catalog Number
T62
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
303cd904-cb9e-4857-9bd7-50e74d88b3ad

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
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 30889483606258
Primary 10889483606254
Previous 10190752145504

Customer Contacts