Duns Number:006261481
Device Description: IPG ATDR01 ATTESTA DR USAA^
Catalog Number
-
Brand Name
Attesta™ DR MRI SureScan™
Version/Model Number
ATDR01
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
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
P980035,P980035
Product Code
LWP
Product Code Name
Implantable pulse generator, pacemaker (non-CRT)
Public Device Record Key
15e9ada2-70bf-4ec2-957d-2a57c8fc1a98
Public Version Date
February 05, 2021
Public Version Number
3
DI Record Publish Date
July 30, 2020
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 |