Catalog Number

000158

Brand Name

GC Fuji IX GP®

Version/Model Number

000158

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

K951555,K951555

Product Code

EMA

Product Code Name

CEMENT, DENTAL

Public Device Record Key

1a6217c3-c659-4ae5-bb74-4e0d235f38c6

Public Version Date

August 29, 2022

Public Version Number

1

DI Record Publish Date

August 19, 2022

Package DI Number

24548161282328

Quantity per Package

5

Contains DI Package

14548161282321

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton