Catalog Number

-

Brand Name

RIVERPOINT BRACHYTHERAPY

Version/Model Number

GM1233-1720

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

IYE

Product Code Name

Accelerator, Linear, Medical

Public Device Record Key

fe44ece1-81e0-4b2d-b46d-98bd7ea9cceb

Public Version Date

June 10, 2022

Public Version Number

5

DI Record Publish Date

October 22, 2015

Package DI Number

20812444022166

Quantity per Package

9

Contains DI Package

00812444022162

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-