Duns Number:830016148
Device Description: 3M™ ESPE™ Vitrebond™ Light Cure Glass Ionomer Liner/Base Powder Refill, 7512P
Catalog Number
7512P
Brand Name
Vitrebond™
Version/Model Number
7512P
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
EMA
Product Code Name
CEMENT, DENTAL
Public Device Record Key
54a162a5-907d-47b2-816d-674c3e75790d
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
August 04, 2017
Package DI Number
50605861012756
Quantity per Package
10
Contains DI Package
30605861012752
Package Discontinue Date
-
Package Status
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 |