Duns Number:058614483
Device Description: Fiducial Marker;Coil
Catalog Number
-
Brand Name
superDimension
Version/Model Number
SDC20
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
April 06, 2018
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
-
Product Code
IYE
Product Code Name
Accelerator, linear, medical
Public Device Record Key
da228c62-f46c-460b-98fe-5e46f61f6778
Public Version Date
June 10, 2022
Public Version Number
8
DI Record Publish Date
September 24, 2016
Package DI Number
20884521198774
Quantity per Package
5
Contains DI Package
10884521198777
Package Discontinue Date
April 06, 2018
Package Status
Not 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 | 132 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 8540 |
| 3 | A medical device with high risk that requires premarket approval | 202 |
| U | Unclassified | 40 |