Duns Number:081305064
Device Description: PIEZO BONE SURGERY TIPS FOR SURGIMASTER AND SURGIMASTER II,DUP1 ROOT SURFACE SCALING, CLEA PIEZO BONE SURGERY TIPS FOR SURGIMASTER AND SURGIMASTER II,DUP1 ROOT SURFACE SCALING, CLEAN
Catalog Number
8150-1
Brand Name
Power Dental USA
Version/Model Number
8150-1
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"
Yes
For Single-Use
-
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
MDM
Product Code Name
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
Public Device Record Key
d60b774b-5f15-48bb-909a-3cf31096335f
Public Version Date
March 24, 2022
Public Version Number
3
DI Record Publish Date
July 13, 2021
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 | 2768 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 18 |