Duns Number:809784593
Device Description: Twist Sterile Female Intermittent Catheter, Straight Tip
Catalog Number
-
Brand Name
CURE TWIST
Version/Model Number
T12
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
K080881,K080881,K080881
Product Code
KOD
Product Code Name
Catheter, Urological
Public Device Record Key
8647e0cc-287d-4312-8f5d-a2373378ab0e
Public Version Date
October 26, 2022
Public Version Number
4
DI Record Publish Date
September 24, 2016
Package DI Number
20815947020387
Quantity per Package
10
Contains DI Package
10815947020380
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 | 18 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 116 |
| U | Unclassified | 8 |