Duns Number:368457563
Device Description: HMEF 1000/S, Disposable
Catalog Number
-
Brand Name
AirLife™
Version/Model Number
557070100
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
f7120ab3-574f-4043-a4a1-8fd4e47b5e8d
Public Version Date
December 22, 2021
Public Version Number
2
DI Record Publish Date
September 01, 2019
Package DI Number
70190752139857
Quantity per Package
50
Contains DI Package
10190752139855
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 13 |
2 | A medical device with a moderate to high risk that requires special controls. | 600 |