Duns Number:009260217
Device Description: Flavored Hemostatic retraction solution for topical dental application with 25% aluminum s Flavored Hemostatic retraction solution for topical dental application with 25% aluminum sulfate, 40 mL
Catalog Number
15610
Brand Name
Retrax Solution 40 mL
Version/Model Number
15610
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
MVL
Product Code Name
Cord, Retraction
Public Device Record Key
fd517246-a38d-4e8b-b5ee-2b88e3a34fb4
Public Version Date
March 04, 2019
Public Version Number
1
DI Record Publish Date
January 30, 2019
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 | 34 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 6 |
| U | Unclassified | 57 |