Catalog Number

-

Brand Name

AirLife™

Version/Model Number

M1003346

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

CAH

Product Code Name

Filter, Bacterial, Breathing-Circuit

Public Device Record Key

ec996f99-51cd-4039-a3de-4059e581ba25

Public Version Date

September 22, 2020

Public Version Number

2

DI Record Publish Date

September 01, 2019

Package DI Number

70190752139789

Quantity per Package

50

Contains DI Package

10190752139787

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-