Catalog Number

-

Brand Name

Philips IntelliVue XDS Application

Version/Model Number

M

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

MSX

Product Code Name

SYSTEM,NETWORK AND COMMUNICATION,PHYSIOLOGICAL MONITORS

Public Device Record Key

5621b589-f679-48d8-bb53-cf69862229c6

Public Version Date

December 07, 2020

Public Version Number

4

DI Record Publish Date

August 25, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-