Catalog Number

-

Brand Name

Medex

Version/Model Number

MX962H182

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"

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

K172458,K172458

Product Code

DRS

Product Code Name

Transducer, blood-pressure, extravascular

Public Device Record Key

a7b5231f-db55-48ba-a9d6-b025885070bf

Public Version Date

July 06, 2018

Public Version Number

4

DI Record Publish Date

November 20, 2017

Package DI Number

35019517082153

Quantity per Package

10

Contains DI Package

15019517082159

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX