Catalog Number

-

Brand Name

Gold Marker

Version/Model Number

GM1233

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K103449,K103449

Product Code

NEU

Product Code Name

Marker, Radiographic, Implantable

Public Device Record Key

b903530c-b1aa-4a6a-a5c3-7e1dd2ed266d

Public Version Date

April 03, 2020

Public Version Number

1

DI Record Publish Date

March 26, 2020

Package DI Number

10810020083146

Quantity per Package

10

Contains DI Package

00810020083149

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-