FDA UDI In Commercial Distribution 🇺🇸 United States

AirLife™

DI: 10889483224151 · Model: 0250 · SUNMED, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
AirLife™
Primary DI
10889483224151
Version / Model
0250
Catalog Number
0250
Company Name
SUNMED, LLC
Labeler DUNS
069009268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-19
Public Version
1
Public Version Date
2025-12-29
Public Version Status
New
Public Device Record Key
f6090201-5ef9-4e45-bf4f-738cccca4e48

Device Description

AirLife™ Aerosol Mask, Adult

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BYG Mask, Oxygen

GMDN Terms

Code Name
35172 Aerosol face mask, non-rebreathing

Identifiers

Type ID
Package 20889483224158
Primary 10889483224151
Previous 00709078003769

Customer Contacts