CoJet™ Sand - 3M™ ESPE™ CoJet™ System Refill, 68411 DM DI = - 3M Deutschland GmbH

Duns Number:315731711

Device Description: 3M™ ESPE™ CoJet™ System Refill, 68411 DM DI = 04035077024167

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More Product Details

Catalog Number

68411

Brand Name

CoJet™ Sand

Version/Model Number

68411

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

KLE

Product Code Name

AGENT, TOOTH BONDING, RESIN

Device Record Status

Public Device Record Key

89a8f5f5-0370-43ab-a464-ba6b401585b1

Public Version Date

December 07, 2018

Public Version Number

3

DI Record Publish Date

August 08, 2017

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