Duns Number:080456871
Device Description: AirLife™ Exhalation Valve One Arm 22 mm I.D., One Arm 22 mm O.D., Closed Stern, Holding Ar AirLife™ Exhalation Valve One Arm 22 mm I.D., One Arm 22 mm O.D., Closed Stern, Holding Arm and 22 mm O.D. Plug
Catalog Number
004379
Brand Name
AirLife™
Version/Model Number
004379
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
BZA
Product Code Name
CONNECTOR, AIRWAY (EXTENSION)
Public Device Record Key
8b102326-377a-4e8a-a470-6b10787cece3
Public Version Date
October 24, 2022
Public Version Number
2
DI Record Publish Date
January 17, 2020
Package DI Number
50190752144734
Quantity per Package
50
Contains DI Package
10190752144736
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 | 1068 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 780 |
| 3 | A medical device with high risk that requires premarket approval | 65 |
| U | Unclassified | 1 |