Primary Device ID | DIVO7409981 |
NIH Device Record Key | 0280ed2d-4d8b-499a-b313-d10b6682214f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BLUEPHASE POWERCURE |
Version Model Number | 740998 |
Catalog Number | 740998 |
Company DUNS | 448015938 |
Company Name | IVOCLAR VIVADENT AKTIENGESELLSCHAFT |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | DIVO7409981 [Primary] |
EBZ | ACTIVATOR, ULTRAVIOLET, FOR POLYMERIZATION |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-03-17 |
Device Publish Date | 2020-03-09 |
DIVO6670931 | Bluephase PowerCure handpiece, Bluephase PowerCure battery, Bluephase PowerCure light guide |
DIVO7409981 | Bluephase G4 handpiece, Bluephase G4 battery, Bluephase G4 light guide |
DVIV691918BU1 | Blueph. PowerCure & System Kit mixed |
DVIV668253BU1 | Bluephase PowerCure & System Kit syringe |
07615208461299 | Bluephase PowerCure 100-240V |
07615208461251 | Bluephase PowerCure 100-240V |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BLUEPHASE POWERCURE 79171560 4985929 Live/Registered |
IVOCLAR VIVADENT AG 2015-05-22 |