Duns Number:926684994
Device Description: Model AT P54, p/n 700608-052Kit Contents: hand controller, 3-way high-pressure stopcock wi Model AT P54, p/n 700608-052Kit 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
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
-
Product Code
DXT
Product Code Name
Injector And Syringe, Angiographic
Public Device Record Key
ba09768d-4489-43a8-acb7-fea48e55f9f2
Public Version Date
September 16, 2022
Public Version Number
3
DI Record Publish Date
March 01, 2018
Package DI Number
30841716100353
Quantity per Package
10
Contains DI Package
10841716100359
Package Discontinue Date
-
Package Status
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 |