Duns Number:606173334
Catalog Number
908124
Brand Name
Radica®
Version/Model Number
Dentin C1
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 05, 2022
Issuing Agency
In HIBCC
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
EBD
Product Code Name
COATING, FILLING MATERIAL, RESIN
Public Device Record Key
ae4a2c01-a723-4b33-852a-ace2df6c03f7
Public Version Date
May 06, 2022
Public Version Number
4
DI Record Publish Date
September 21, 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 | 57 |
2 | A medical device with a moderate to high risk that requires special controls. | 19532 |