Duns Number:830432451
Device Description: Airlife™ MM10 SVN, 7' O2 Tube, Valved Tee 22 mm OD/ID
Catalog Number
ANEV20110A
Brand Name
AirLife
Version/Model Number
ANEV20110A
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
OGG
Product Code Name
Humidifier nebulizer kit
Public Device Record Key
d368921d-d1ef-48c5-b96a-204fde5ffb87
Public Version Date
August 05, 2022
Public Version Number
4
DI Record Publish Date
September 01, 2016
Package DI Number
50885403184275
Quantity per Package
16
Contains DI Package
10885403184277
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 |