Duns Number:659177273
Device Description: The Venner™ PneuX P.Y.™ Endotracheal tube is designed to be used for patients undergoing T
Catalog Number
901180
Brand Name
Venner™ PneuX P.Y.™ ETT MRI
Version/Model Number
901180
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
Yes
FDA Premarket Submission
K093135,K093135,K093135
Product Code
BTR
Product Code Name
Tube, Tracheal (W/Wo Connector)
Public Device Record Key
fcf6bcaf-5396-4662-bcfd-ddf0333a23e1
Public Version Date
May 06, 2019
Public Version Number
3
DI Record Publish Date
September 24, 2016
Package DI Number
28885009190770
Quantity per Package
10
Contains DI Package
18885009190773
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
10 boxes in a carton
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 20 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 7 |