Duns Number:002348191
Device Description: 14FR Standard Female
Catalog Number
SONC-14F
Brand Name
RUSCH
Version/Model Number
IPN039327
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
K010420,K010420,K010420
Product Code
KOD
Product Code Name
CATHETER, UROLOGICAL
Public Device Record Key
b6d71176-b753-4eaf-b063-bf0f4139d064
Public Version Date
January 18, 2021
Public Version Number
6
DI Record Publish Date
June 11, 2019
Package DI Number
24026704662085
Quantity per Package
100
Contains DI Package
14026704662088
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 | 3195 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 13747 |
| 3 | A medical device with high risk that requires premarket approval | 3 |
| U | Unclassified | 26 |