Bluephase PowerCure 667092AA
GUDID 07615208461251
Bluephase PowerCure 100-240V
IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp Dental/surgical polymerization lamp| Primary Device ID | 07615208461251 |
| NIH Device Record Key | 4c6bd093-3d37-488d-8e25-0dfdc208d2d7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bluephase PowerCure |
| Version Model Number | 667092AA |
| Catalog Number | 667092AA |
| 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 | true |
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07615208458787 [Primary] |
| GS1 | 07615208461251 [Direct Marking] |
FDA Product Code
| EBZ | ACTIVATOR, ULTRAVIOLET, FOR POLYMERIZATION |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
[07615208461251]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-04-02 |
| Device Publish Date | 2024-03-25 |
On-Brand Devices [Bluephase PowerCure]
| 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 |
Trademark Results [Bluephase PowerCure]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BLUEPHASE POWERCURE 79171560 4985929 Live/Registered |
IVOCLAR VIVADENT AG 2015-05-22 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.