Duns Number:926684994
Device Description: Model AT P54, p/n 700608-048Kit Contents: hand controller, 3-way high-pressure stopcock wi Model AT P54, p/n 700608-048Kit Contents: hand controller, 3-way high-pressure stopcock with rotating end and premium high-pressure tubing
Catalog Number
-
Brand Name
AngioTouch® Kit
Version/Model Number
014644
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 21, 2018
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
-
Product Code
DXT
Product Code Name
Injector And Syringe, Angiographic
Public Device Record Key
0d9fbc7c-ba2f-4f53-8a63-a54cb87bd752
Public Version Date
September 16, 2022
Public Version Number
4
DI Record Publish Date
September 09, 2016
Package DI Number
30841716101305
Quantity per Package
10
Contains DI Package
10841716101301
Package Discontinue Date
May 21, 2018
Package Status
Not in Commercial Distribution
Package Type
Shelf box
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 193 |