Duns Number:448015938
Device Description: Bluephase PowerCure handpiece w. light guide
Catalog Number
740998
Brand Name
BLUEPHASE POWERCURE
Version/Model Number
740998
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 18, 2022
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
-
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
EBZ
Product Code Name
ACTIVATOR, ULTRAVIOLET, FOR POLYMERIZATION
Public Device Record Key
0280ed2d-4d8b-499a-b313-d10b6682214f
Public Version Date
May 19, 2022
Public Version Number
3
DI Record Publish Date
March 09, 2020
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 | 131 |
2 | A medical device with a moderate to high risk that requires special controls. | 12768 |