Duns Number:140727624
Device Description: One-Piece/Tuohy-Borst Catheter Introducer Kit 8F
Catalog Number
A497444
Brand Name
One-Piece/Tuohy-Borst Catheter Introducer Kit
Version/Model Number
A497444
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
K780126,K780126
Product Code
DRE
Product Code Name
Dilator, Vessel, For Percutaneous Catheterization
Public Device Record Key
a4d80945-0719-4b96-9fea-a5485ae3af8b
Public Version Date
June 07, 2019
Public Version Number
4
DI Record Publish Date
September 12, 2016
Package DI Number
20886333216417
Quantity per Package
10
Contains DI Package
00886333216413
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 | 347 |
2 | A medical device with a moderate to high risk that requires special controls. | 1205 |