Duns Number:038305402
Device Description: Anti-Static Spacer w/ Medium O2 Mask
Catalog Number
-
Brand Name
Ventlab
Version/Model Number
BR320
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
f5fa1571-b169-4a3e-beea-957a8b6b2e54
Public Version Date
June 08, 2021
Public Version Number
3
DI Record Publish Date
October 01, 2016
Package DI Number
20889483093396
Quantity per Package
20
Contains DI Package
10889483093399
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 82 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 612 |