Duns Number:006261481
Device Description: LEAD 5076-85 MRI US RCMCRD
Catalog Number
-
Brand Name
CapSureFix Novus MRI™ SureScan®
Version/Model Number
5076-85
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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"
-
For Single-Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
P930039
Product Code
DTB
Product Code Name
permanent pacemaker Electrode
Public Device Record Key
95e71e48-983e-4fac-a44c-05ad68e35056
Public Version Date
February 05, 2021
Public Version Number
4
DI Record Publish Date
June 02, 2017
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 | 102 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 20495 |
| 3 | A medical device with high risk that requires premarket approval | 3601 |