Duns Number:830432451
Device Description: Airlife™ Isothermal™ Breathing Circuit Accessory - 10mm Nebulizer Adapter
Catalog Number
4220-504
Brand Name
AirLife
Version/Model Number
4220-504
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"
Yes
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
CAF
Product Code Name
NEBULIZER (DIRECT PATIENT INTERFACE)
Public Device Record Key
74149091-7750-41cc-a429-9eb56a9fce10
Public Version Date
October 24, 2022
Public Version Number
5
DI Record Publish Date
September 01, 2016
Package DI Number
50885403167704
Quantity per Package
30
Contains DI Package
10885403167706
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 2 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 876 |
| 3 | A medical device with high risk that requires premarket approval | 29 |