Duns Number:134139174
Device Description: Blood Management System
Catalog Number
48VMPL120
Brand Name
VAMP
Version/Model Number
48VMPL120
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Safe
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
K161962,K161962
Product Code
KRA
Product Code Name
Catheter, Continuous Flush
Public Device Record Key
552386b7-207a-4308-a3f8-a4be6ff30723
Public Version Date
April 25, 2019
Public Version Number
1
DI Record Publish Date
April 17, 2019
Package DI Number
50690103200299
Quantity per Package
20
Contains DI Package
00690103200294
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Shipper
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 5 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 643 |
| 3 | A medical device with high risk that requires premarket approval | 212 |