Duns Number:144140845
Device Description: NUPRO® 5% Sodium Fluoride White Varnish, Patient Dose Kit - Grape. Contents: 100 Patient D NUPRO® 5% Sodium Fluoride White Varnish, Patient Dose Kit - Grape. Contents: 100 Patient Doses of 0.4g, 100 Brush applicators and 1 Prophy Grip.
Catalog Number
-
Brand Name
NUPRO®
Version/Model Number
130211
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
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
LBH
Product Code Name
VARNISH, CAVITY
Public Device Record Key
a098265b-8e44-4324-91c8-1236e5fd35f8
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
September 23, 2016
Package DI Number
D0031302112
Quantity per Package
4
Contains DI Package
D0031302111
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 13 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 156 |