Duns Number:448015938
Device Description: Proxyt Test Pack RDA 7 Fein 10 ml
Catalog Number
601603
Brand Name
Proxyt
Version/Model Number
601603
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 31, 2021
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
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
-
Product Code
EJR
Product Code Name
AGENT, POLISHING, ABRASIVE, ORAL CAVITY
Public Device Record Key
aedfea3a-e123-44f0-9da4-0e4760c6a267
Public Version Date
September 01, 2021
Public Version Number
2
DI Record Publish Date
August 26, 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 | 131 |
2 | A medical device with a moderate to high risk that requires special controls. | 12768 |