Catalog Number

-

Brand Name

Merge Unity PACS

Version/Model Number

13.0

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 21, 2021

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K041935

Product Code

LLZ

Product Code Name

System, Image Processing, Radiological

Public Device Record Key

09aebb0a-2e94-4827-9435-bac458a2bdcd

Public Version Date

January 14, 2022

Public Version Number

2

DI Record Publish Date

September 21, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-