FDA UDI In Commercial Distribution 🇺🇸 United States

AirLife™

DI: 10889483570890 · Model: 002002 · AIRLIFE
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
AirLife™
Primary DI
10889483570890
Version / Model
002002
Catalog Number
002002
Company Name
AIRLIFE
Labeler DUNS
119058668
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-02-20
Public Version
3
Public Version Date
2025-09-24
Public Version Status
Update
Public Device Record Key
442d5cb7-b2ba-42d6-8d81-64f68d654878

Device Description

AirLife™ Nebulizer with Air Entrainment

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

Code Name
35457 Therapeutic agent nebulizer, benchtop

Identifiers

Type ID
Package 30889483570894
Primary 10889483570890
Previous 10190752144798

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K801252 000