Duns Number:838024255
Device Description: 21G x 3/4" w/7" tubing VanishPoint® Blood Collection Set
Catalog Number
24031
Brand Name
VanishPoint®
Version/Model Number
24031
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
FPA
Product Code Name
Set, Administration, Intravascular
Public Device Record Key
93208115-23f9-4629-b34b-30ab58b060b1
Public Version Date
April 07, 2021
Public Version Number
3
DI Record Publish Date
September 22, 2016
Package DI Number
00613703240323
Quantity per Package
4
Contains DI Package
00613703240316
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 77 |