FDA UDI In Commercial Distribution 🇺🇸 United States

AirLife™

DI: 10889483581995 · Model: 4023RH · AIRLIFE
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
10889483581995
Version / Model
4023RH
Catalog Number
4023RH
Company Name
AIRLIFE
Labeler DUNS
119058668
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-12
Public Version
2
Public Version Date
2025-04-17
Public Version Status
Update
Public Device Record Key
24cd027e-a220-44ce-8e6c-b9763d42b779

Device Description

Reduced Heparin (Arterial Blood Sampler)

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
CBT Arterial blood sampling kit

GMDN Terms

Code Name
31336 Arterial blood sampling kit

Identifiers

Type ID
Primary 10889483581995
Previous 10885403271656

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K822786 000