Duns Number:305524696
Device Description: SILICONE Double loop ureteral stent open/open CH FR 06 length 26 cm with connectable pushe SILICONE Double loop ureteral stent open/open CH FR 06 length 26 cm with connectable pusher CH FR 06 and Orchestra™ guidewire
Catalog Number
AJ5064
Brand Name
Porges Coloplast
Version/Model Number
AJ5064
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
K013921
Product Code
FAD
Product Code Name
STENT, URETERAL
Public Device Record Key
428709e6-d1fd-49db-886b-86e32ce1dc7f
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 24, 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 | 46 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 899 |
| 3 | A medical device with high risk that requires premarket approval | 72 |
| U | Unclassified | 7 |