Catalog Number

-

Brand Name

SONIC SHOT GX

Version/Model Number

070

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

-

Product Code

IZQ

Product Code Name

Injector, Contrast Medium, Automatic

Public Device Record Key

94cc4ddd-481a-445c-a271-b3cb061ae886

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

July 15, 2016

Package DI Number

14560138480707

Quantity per Package

1

Contains DI Package

04560138480700

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-