FDA UDI In Commercial Distribution 🇺🇸 United States

AirLife™

DI: 10190752114357 · Model: 2K8032M · AIRLIFE
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
AirLife™
Primary DI
10190752114357
Version / Model
2K8032M
Catalog Number
2K8032M
Company Name
AIRLIFE
Labeler DUNS
119058668
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-22
Public Version
3
Public Version Date
2025-04-17
Public Version Status
Update
Public Device Record Key
50e92d8b-ae3c-40d8-b511-9a29a313a721

Device Description

Adult Manual Resuscitator

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
No
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 50190752114355
Primary 10190752114357

Customer Contacts