FDA UDI In Commercial Distribution 🇺🇸 United States

AirLife™

DI: 10190752114333 · Model: 2K8021 · VYAIRE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
AirLife™
Primary DI
10190752114333
Version / Model
2K8021
Catalog Number
2K8021
Company Name
VYAIRE MEDICAL, INC.
Labeler DUNS
080456871
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-02-04
Public Version
1
Public Version Date
2020-02-12
Public Version Status
New
Public Device Record Key
6edceed9-e45a-43ae-92e2-5e25b4274e4c

Device Description

AirLife™ Infant Manual Resuscitator Oxygen Reservoir Bag, Pressure Limiting Valve with Lock

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
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
OFP Anesthesia breathing circuit kit (adult & pediatric)

GMDN Terms

Code Name
36086 Pulmonary resuscitator, manual, single-use

Identifiers

Type ID
Package 50190752114331
Primary 10190752114333

Customer Contacts

Device Sizes

Type Value Unit Text
Weight 0.33 Kilogram
Total Volume 600 Milliliter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 60 Degrees Celsius