FDA UDI In Commercial Distribution 🇺🇸 United States

AirLife™

DI: 10190752145757 · Model: 5514RESP · VYAIRE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
AirLife™
Primary DI
10190752145757
Version / Model
5514RESP
Catalog Number
5514RESP
Company Name
VYAIRE MEDICAL, INC.
Labeler DUNS
080456871
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-01-15
Public Version
1
Public Version Date
2020-01-23
Public Version Status
New
Public Device Record Key
a775e1ea-656f-4f98-86bc-d82d54509bad

Device Description

AirLife™ baby safe flow-inflating resuscitation device 1/2 Liter Bag

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BZD VENTILATOR, NON-CONTINUOUS (RESPIRATOR)

GMDN Terms

Code Name
36086 Pulmonary resuscitator, manual, single-use

Identifiers

Type ID
Package 50190752145755
Primary 10190752145757

Customer Contacts