Duns Number:830016148
Device Description: 3M™ ESPE™ Filtek™ Supreme Ultra Flowable Restorative Refill, 20 - 0.2g Capsules - D2, 6033 3M™ ESPE™ Filtek™ Supreme Ultra Flowable Restorative Refill, 20 - 0.2g Capsules - D2, 6033D2
Catalog Number
6033D2
Brand Name
Filtek™
Version/Model Number
6033D2
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
February 13, 2017
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
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
EBF
Product Code Name
MATERIAL, TOOTH SHADE, RESIN
Public Device Record Key
17f25a88-f0a8-4968-b8f8-0a54fcac1752
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
September 24, 2016
Package DI Number
50605861061662
Quantity per Package
10
Contains DI Package
30605861061668
Package Discontinue Date
February 13, 2017
Package Status
Not in Commercial Distribution
Package Type
BOX
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 274 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 444 |
| U | Unclassified | 7 |