FDA UDI In Commercial Distribution 🇺🇸 United States

AirLife

DI: 10885403223174 · Model: 2K80232 · Carefusion Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
AirLife
Primary DI
10885403223174
Version / Model
2K80232
Catalog Number
2K80232
Company Name
Carefusion Corporation
Labeler DUNS
830432451
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
8cc2e645-0886-48a2-bb72-6cc610b0b26a

Device Description

1/4 Liter Neoprene Flow-Inflating Bag with Pre-Attached 7’ (2.1 m) Oxygen Tubing and Manometer

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OEV Cardiopulmonary Resuscitation Aid Kit

GMDN Terms

Code Name
36086 Pulmonary resuscitator, manual, single-use

Identifiers

Type ID
Package 50885403223172
Primary 10885403223174

Customer Contacts

Phone
800.323.9088

Device Sizes

Type Value Unit Text
Total Volume .25 Liter