Catalog Number

-

Brand Name

Injector Head

Version/Model Number

102410

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

IZQ

Product Code Name

Injector, Contrast Medium, Automatic

Public Device Record Key

aa90bee4-c729-4f0b-8455-e96ddbb52653

Public Version Date

March 15, 2021

Public Version Number

1

DI Record Publish Date

March 05, 2021

Package DI Number

37630039300891

Quantity per Package

1

Contains DI Package

17630039300910

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

box