FDA UDI In Commercial Distribution 🇺🇸 United States

AirLife

DI: 70885403276578 · Model: 172230 · Carefusion Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
AirLife
Primary DI
70885403276578
Version / Model
172230
Catalog Number
172230
Company Name
Carefusion Corporation
Labeler DUNS
830432451
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2016-09-21
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
0230b01d-a09b-48f3-8f2d-185760cca5d8

Device Description

AirLife&#8482 One-way valve 22 mm ID x 22 mm OD with directional idicator arrow

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CAF NEBULIZER (DIRECT PATIENT INTERFACE)

GMDN Terms

Code Name
60657 Non-rebreathing valve, single-use

Identifiers

Type ID
Primary 70885403276578
Unit of Use 10885403276576

Customer Contacts