FDA UDI In Commercial Distribution 🇺🇸 United States

AirLife™

DI: 10889483579466 · Model: 2D0735X · 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
10889483579466
Version / Model
2D0735X
Catalog Number
2D0735X
Company Name
AIRLIFE
Labeler DUNS
119058668
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-02-12
Public Version
3
Public Version Date
2026-04-20
Public Version Status
Update
Public Device Record Key
85d3b843-de2c-4eb8-a0a0-43b0acabb0dc

Device Description

Sterile Water for Inhalation

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
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
BTT Humidifier, Respiratory Gas, (Direct Patient Interface)

GMDN Terms

Code Name
44706 Inhalation therapy sterile water

Identifiers

Type ID
Package 30889483579460
Primary 10889483579466
Previous 10190752196445

Customer Contacts