GC Fuji II LC® - GC Fuji II LC® B4, 15 g powder btl - Gc America Inc.

Duns Number:005473608

Device Description: GC Fuji II LC® B4, 15 g powder btl

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More Product Details

Catalog Number

000202

Brand Name

GC Fuji II LC®

Version/Model Number

000202

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

8e50f9e7-6ee7-4f6f-996b-51b82854898c

Public Version Date

August 29, 2022

Public Version Number

1

DI Record Publish Date

August 19, 2022

Additional Identifiers

Package DI Number

24548161293638

Quantity per Package

5

Contains DI Package

14548161293631

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton

"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