BLUEPHASE POWERCURE - Bluephase PowerCure & System Kit syringe - IVOCLAR VIVADENT AKTIENGESELLSCHAFT

Duns Number:448015938

Device Description: Bluephase PowerCure & System Kit syringe

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More Product Details

Catalog Number

668253BU

Brand Name

BLUEPHASE POWERCURE

Version/Model Number

668253BU

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 15, 2022

Issuing Agency

In HIBCC

Product Characteristics

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 Details

Product Code

EBZ

Product Code Name

ACTIVATOR, ULTRAVIOLET, FOR POLYMERIZATION

Device Record Status

Public Device Record Key

0cbbf2d6-902c-4726-8320-682b4306fcd5

Public Version Date

March 16, 2022

Public Version Number

2

DI Record Publish Date

December 02, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"IVOCLAR VIVADENT AKTIENGESELLSCHAFT" Characteristics
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