Duns Number:038000253
Device Description: 0.030" BARBED TUNNELER0.030" BAR FOR 3F VASCU-LINE®
Catalog Number
DTUN3
Brand Name
TUNNELERTUNNELER
Version/Model Number
DTUN3
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
MZY
Product Code Name
Graft, vascular, stainless steel tunneler
Public Device Record Key
6a373c8e-18f5-4a6d-aba1-e1af2dc98370
Public Version Date
August 26, 2019
Public Version Number
1
DI Record Publish Date
August 17, 2019
Package DI Number
50884908142056
Quantity per Package
5
Contains DI Package
00884908142051
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 | 31 |
2 | A medical device with a moderate to high risk that requires special controls. | 2560 |