Catalog Number

-

Brand Name

DICOM Proxy

Version/Model Number

4.1

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)

-

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

a006ba7d-e12b-4278-a6d9-1ed02b703f6d

Public Version Date

June 07, 2018

Public Version Number

1

DI Record Publish Date

May 07, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-