Duns Number:017246562
Device Description: ST SORB 2000 W/NOTCH 3 3/4' X 7 1/2'
Catalog Number
SV48VXT-6
Brand Name
Centurion
Version/Model Number
SV48VXT-6
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
KMK
Product Code Name
DEVICE, INTRAVASCULAR CATHETER SECUREMENT
Public Device Record Key
7039a2f9-b6ed-43f2-8924-a9a4a6e2aff6
Public Version Date
January 10, 2022
Public Version Number
1
DI Record Publish Date
January 02, 2022
Package DI Number
00653160270396
Quantity per Package
50
Contains DI Package
10653160270393
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 6043 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 4077 |
| U | Unclassified | 1 |