Variolink Esthetic - Variolink Esthetic DC Neutral, Variolink Esthetic - IVOCLAR VIVADENT AKTIENGESELLSCHAFT

Duns Number:448015938

Device Description: Variolink Esthetic DC Neutral, Variolink Esthetic Try-In Paste Neutral, Adhese Universal V Variolink Esthetic DC Neutral, Variolink Esthetic Try-In Paste Neutral, Adhese Universal VivaPen, Monobond Plus, Liquid Strip, Application Tips Variolink, VivaPen Brush Cannulas, VivaPen Protective Sleeves, Mixing Tips, Various accessories

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More Product Details

Catalog Number

687593WW

Brand Name

Variolink Esthetic

Version/Model Number

687593WW

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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

EBF

Product Code Name

MATERIAL, TOOTH SHADE, RESIN

Device Record Status

Public Device Record Key

7ce102f6-9e5d-4cf7-bb4b-6ce5210efe39

Public Version Date

October 29, 2018

Public Version Number

1

DI Record Publish Date

September 27, 2018

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