Catalog Number

-

Brand Name

Medex

Version/Model Number

MXG300243R1

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"

Yes

For Single-Use

Yes

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

K942377,K942377

Product Code

DPT

Product Code Name

PROBE, BLOOD-FLOW, EXTRAVASCULAR

Public Device Record Key

4b07b631-558a-4452-9008-faedc99e7abe

Public Version Date

July 06, 2018

Public Version Number

4

DI Record Publish Date

October 13, 2016

Package DI Number

50351688518123

Quantity per Package

10

Contains DI Package

10351688518125

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE