Duns Number:315620229
Catalog Number
377177
Brand Name
Solia
Version/Model Number
S 53
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
-
Product Code
NVN
Product Code Name
Drug eluting permanent right ventricular (RV) or right atrial (RA) pacemaker electrodes
Public Device Record Key
af93e6f6-9f64-4132-af32-9ba2e18650d4
Public Version Date
February 05, 2021
Public Version Number
3
DI Record Publish Date
June 17, 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 | 1 |
2 | A medical device with a moderate to high risk that requires special controls. | 97 |
3 | A medical device with high risk that requires premarket approval | 402 |