Duns Number:343689704
Device Description: DIACAP HIPS 12 PS DIALYZER
Catalog Number
7204101
Brand Name
Diacap®
Version/Model Number
7204101
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
February 09, 2019
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
FJI
Product Code Name
DIALYZER, CAPILLARY, HOLLOW FIBER
Public Device Record Key
2d40dcf7-6ead-4a28-866c-6a4eef700205
Public Version Date
August 20, 2021
Public Version Number
5
DI Record Publish Date
August 09, 2015
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 2 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 69 |
| 3 | A medical device with high risk that requires premarket approval | 1 |