FDA UDI In Commercial Distribution 🇺🇸 United States

AirLife™

DI: 10190752114432 · Model: 2K8037 · VYAIRE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
AirLife™
Primary DI
10190752114432
Version / Model
2K8037
Catalog Number
2K8037
Company Name
VYAIRE MEDICAL, INC.
Labeler DUNS
080456871
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-20
Public Version
3
Public Version Date
2020-01-28
Public Version Status
Update
Public Device Record Key
15132b8e-a737-492c-a006-64f3aaef1680

Device Description

AirLife™ Pediatric Manual Resuscitator; 40"(1.0m) Oxygen Resevoir Tubing, PEEP Valve, Pediatric Mask, 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
Yes
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
35425 Non-rebreathing valve, reusable

Identifiers

Type ID
Primary 10190752114432
Package 50190752114430

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 1000.00 Milliliter
Weight .40 Kilogram

Storage Conditions

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