Vitrebond™ - 3M™ ESPE™ Vitrebond™ Plus Light Cure Glass - 3M COMPANY

Duns Number:830016148

Device Description: 3M™ ESPE™ Vitrebond™ Plus Light Cure Glass Ionomer Liner/Base Double Pack Refill, 7572

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More Product Details

Catalog Number

7572

Brand Name

Vitrebond™

Version/Model Number

7572

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

EMA

Product Code Name

CEMENT, DENTAL

Device Record Status

Public Device Record Key

d9c5bd8f-1982-4c67-8aec-6b8098a11c8e

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

August 04, 2017

Additional Identifiers

Package DI Number

50605861012671

Quantity per Package

10

Contains DI Package

30605861012677

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX

"3M COMPANY" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 274
2 A medical device with a moderate to high risk that requires special controls. 444
U Unclassified 7