Duns Number:134139174
Device Description: AVID DUAL STAGE VENOUS DRAINAGE CANNULA
Catalog Number
TF3646O2
Brand Name
AViD Dual Stage Venous Drainage Cannula
Version/Model Number
TF3646O2
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"
-
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
K120072,K120072
Product Code
DWF
Product Code Name
CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS
Public Device Record Key
e50b11e0-4134-4bab-99a5-6dcaa06517ea
Public Version Date
August 05, 2022
Public Version Number
4
DI Record Publish Date
August 31, 2016
Package DI Number
50690103160425
Quantity per Package
10
Contains DI Package
00690103160420
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 5 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 643 |
| 3 | A medical device with high risk that requires premarket approval | 212 |