Ketac™ Molar Aplicap™ - 3M™ ESPE™ Ketac™ Molar Aplicap™ Glass Ionomer - 3M Deutschland GmbH

Duns Number:315731711

Device Description: 3M™ ESPE™ Ketac™ Molar Aplicap™ Glass Ionomer Restorative Material Refill, 56433

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More Product Details

Catalog Number

56433

Brand Name

Ketac™ Molar Aplicap™

Version/Model Number

56433

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

Yes

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

EMA

Product Code Name

CEMENT, DENTAL

Device Record Status

Public Device Record Key

9c293141-ff4a-414c-a9aa-f5d8cbee2c2e

Public Version Date

December 10, 2018

Public Version Number

4

DI Record Publish Date

September 24, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"3M DEUTSCHLAND GMBH" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 232
2 A medical device with a moderate to high risk that requires special controls. 563
U Unclassified 3