Catalog Number

-

Brand Name

GOLD MARKER NEEDLE

Version/Model Number

GM1054-1825

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,K103449,K103449

Product Code

KXK

Product Code Name

Source, Brachytherapy, Radionuclide

Public Device Record Key

7a47cae1-327b-42a9-903e-734cd39fa13b

Public Version Date

July 12, 2018

Public Version Number

4

DI Record Publish Date

July 18, 2016

Package DI Number

20812444025785

Quantity per Package

9

Contains DI Package

00812444025781

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-