FDA UDI In Commercial Distribution 🇺🇸 United States

AirLife™

DI: 10889483569443 · Model: 001240 · 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
10889483569443
Version / Model
001240
Catalog Number
001240
Company Name
AIRLIFE
Labeler DUNS
119058668
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-02-19
Public Version
2
Public Version Date
2025-04-17
Public Version Status
Update
Public Device Record Key
9b4ce1e8-9b56-4b71-96ea-c49d34c6ad1c

Device Description

AirLife™ Adult Venturi Style Mask Vinyl, Under-the-Chin Style

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
CAT Cannula, Nasal, Oxygen

GMDN Terms

Code Name
35175 Venturi oxygen face mask

Identifiers

Type ID
Package 30889483569447
Primary 10889483569443
Previous 10190752116443

Customer Contacts