Catalog Number

A280-0585

Brand Name

IMAGE DIAGNOSTICS, INC.

Version/Model Number

MDS-D, 230V

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

April 18, 2018

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LMD

Product Code Name

System, Digital Image Communications, Radiological

Public Device Record Key

f29cc7d8-952b-4dda-9f41-826e5fe13601

Public Version Date

October 24, 2022

Public Version Number

4

DI Record Publish Date

August 02, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-