FDA UDI In Commercial Distribution 🇺🇸 United States

AirLife™

DI: 10190752156487 · Model: 2K80293 · VYAIRE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
AirLife™
Primary DI
10190752156487
Version / Model
2K80293
Catalog Number
2K80293
Company Name
VYAIRE MEDICAL, INC.
Labeler DUNS
080456871
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-03
Public Version
1
Public Version Date
2021-05-11
Public Version Status
New
Public Device Record Key
128e4780-a53e-4140-8b5a-1506acd55b34

Device Description

2 Liter Neoprene Flow-Inflating Bag with Pre-Attached 7’ (2.1 m) Oxygen Tubing, Manometer and Small Adult Valved Mask

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
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 50190752156485
Primary 10190752156487

Customer Contacts