Duns Number:184763290
Catalog Number
CSS-362
Brand Name
Peritoneal Dialysis
Version/Model Number
00884450462782
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
FKX
Product Code Name
System, peritoneal, automatic delivery
Public Device Record Key
a0de78ad-7753-4ffd-9b26-267093cc1057
Public Version Date
November 10, 2021
Public Version Number
3
DI Record Publish Date
June 03, 2021
Package DI Number
10884450462789
Quantity per Package
1
Contains DI Package
00884450462782
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 573 |
2 | A medical device with a moderate to high risk that requires special controls. | 8779 |