Catalog Number

-

Brand Name

Medex

Version/Model Number

MX95020

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

-

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

Product Code

DPT

Product Code Name

PROBE, BLOOD-FLOW, EXTRAVASCULAR

Public Device Record Key

710d8a47-03d0-4106-bbd8-8fab2a136903

Public Version Date

July 06, 2018

Public Version Number

4

DI Record Publish Date

October 12, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-