Catalog Number

-

Brand Name

Medical Imaging Solutions Intl.

Version/Model Number

200111

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K152906,K152906

Product Code

DXT

Product Code Name

Injector And Syringe, Angiographic

Public Device Record Key

21ba3ffd-b51c-44c4-adf6-b97a2fb914cf

Public Version Date

January 25, 2021

Public Version Number

1

DI Record Publish Date

January 15, 2021

Package DI Number

10850014500365

Quantity per Package

50

Contains DI Package

00850014500368

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case