Duns Number:160032025
Device Description: SIGNA Premier System Medical Device Assembly, MDR
Catalog Number
-
Brand Name
NA
Version/Model Number
SIGNA Premier
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
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"
-
For Single-Use
-
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K193282
Product Code
LNH
Product Code Name
System, nuclear magnetic resonance imaging
Public Device Record Key
332dd2de-774f-4fc4-b60d-ce7b39ab6ecc
Public Version Date
May 26, 2022
Public Version Number
2
DI Record Publish Date
August 14, 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 | 1 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 81 |