Duns Number:958291411
Device Description: Pre-pump, 8.0 mm, with Twister® Reverse Access Flow Device
Catalog Number
03-2794-0
Brand Name
CombiSet Twister
Version/Model Number
03-2794-0
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
K022536,K022536
Product Code
KOC
Product Code Name
ACCESSORIES, BLOOD CIRCUIT, HEMODIALYSIS
Public Device Record Key
3dfa9781-f532-40b1-8770-a70c8ada49d6
Public Version Date
June 07, 2019
Public Version Number
4
DI Record Publish Date
September 24, 2015
Package DI Number
10840861100313
Quantity per Package
24
Contains DI Package
00840861100316
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 65 |