Duns Number:038000253
Device Description: 13F X 15CM DUO-SPLIT®IJ CATHETER SETCATHETER SET
Catalog Number
DDSP136IJS
Brand Name
DUO-SPLIT®
Version/Model Number
DDSP136IJS
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
MPB
Product Code Name
CATHETER, HEMODIALYSIS, NON-IMPLANTED
Public Device Record Key
c87fcac6-add2-4786-880b-028f2be15136
Public Version Date
February 05, 2021
Public Version Number
2
DI Record Publish Date
August 14, 2019
Package DI Number
50884908145828
Quantity per Package
5
Contains DI Package
00884908145823
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 | 31 |
2 | A medical device with a moderate to high risk that requires special controls. | 2560 |