Duns Number:830432451
Device Description: Airlife™ Universal IPPB Manifold and Nebulizer with 39" (1.0 m), 22 mm I.D. Aerosol Airlife™ Universal IPPB Manifold and Nebulizer with 39" (1.0 m), 22 mm I.D. Aerosol Tube, Two Supply Lines, Mouthpiece, and 6" (15 cm), 22 mm I.D. Flextube
Catalog Number
001608
Brand Name
AirLife
Version/Model Number
001608
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
396a9953-7691-4a68-aa89-195d5fc1b6e3
Public Version Date
June 10, 2022
Public Version Number
4
DI Record Publish Date
September 01, 2016
Package DI Number
50885403163980
Quantity per Package
50
Contains DI Package
10885403163982
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 |