Duns Number:355280827
Device Description: Set of 2 UDI products as a convenience kit
Catalog Number
514-50-3SR041
Brand Name
imagiQ
Version/Model Number
Hand control holder US
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
-
Product Code
CDG
Product Code Name
Chromatography Separation/Zimmerman 17-Ketogenic Steroids
Public Device Record Key
61309d34-94da-4f25-b16e-0f7f37e6ab20
Public Version Date
March 22, 2021
Public Version Number
1
DI Record Publish Date
March 12, 2021
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 | 1073 |
2 | A medical device with a moderate to high risk that requires special controls. | 17 |