Duns Number:006261481
Device Description: LEAD 429678 MRI CANT US
Catalog Number
-
Brand Name
Attain Ability™ Plus MRI SureScan™
Version/Model Number
429678
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
April 15, 2021
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
P080006,P080006
Product Code
DTB
Product Code Name
permanent pacemaker Electrode
Public Device Record Key
284f1b92-44fc-4e5a-bb95-bd6921aadda2
Public Version Date
January 31, 2022
Public Version Number
6
DI Record Publish Date
February 26, 2016
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 |