Duns Number:140727624
Device Description: Vesselpaws, Blue Maxi
Catalog Number
001-1-620
Brand Name
Vesselpaws, Blue Maxi
Version/Model Number
001-1-620
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
DXC
Product Code Name
Clamp, Vascular
Public Device Record Key
93c72772-f6af-4cbe-9217-690863d28ec3
Public Version Date
May 06, 2020
Public Version Number
4
DI Record Publish Date
September 23, 2016
Package DI Number
20886333222999
Quantity per Package
100
Contains DI Package
00886333222995
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 |