MI Paste Plus™ - MI Paste Plus™ 10 tubes (40g each) Vanilla only - Gc America Inc.

Duns Number:005473608

Device Description: MI Paste Plus™ 10 tubes (40g each) Vanilla only

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More Product Details

Catalog Number

422888

Brand Name

MI Paste Plus™

Version/Model Number

422888

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

K070854,K070854

Product Code Details

Product Code

EJR

Product Code Name

AGENT, POLISHING, ABRASIVE, ORAL CAVITY

Device Record Status

Public Device Record Key

70cf9efc-e216-4b8b-baae-eea508e949a0

Public Version Date

February 07, 2019

Public Version Number

4

DI Record Publish Date

February 10, 2017

Additional Identifiers

Package DI Number

D6584228882

Quantity per Package

30

Contains DI Package

D6584228881

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-

"GC AMERICA INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 480
2 A medical device with a moderate to high risk that requires special controls. 4772