FDA UDI In Commercial Distribution 🇺🇸 United States

AirLife™

DI: 10190752141285 · Model: 2K7000 · VYAIRE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
AirLife™
Primary DI
10190752141285
Version / Model
2K7000
Catalog Number
2K7000
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
21e2f03d-a260-4ff5-af72-37bad41db3eb

Device Description

Manual Resuscitator II

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 50190752141290
Primary 10190752141285

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 50 Degrees Celsius