PHILIPS IntelliVue MX700 patient monitor - The IntelliVue MX700 patient monitor is operated - Philips Medizin Systeme Böblingen GmbH

Duns Number:314101143

Device Description: The IntelliVue MX700 patient monitor is operated primarily via touchscreen. It has an inte The IntelliVue MX700 patient monitor is operated primarily via touchscreen. It has an integrated 15" TFT widescreen touch display. It is compatible with the MMS (M3001A) / X2 (M3002A) Multi-Measurement Modules/ all Multi-measurement module extensions/ IntelliVue MMX (867036)/ IntelliVue X3 (867030), the FMS Module Racks (FMS-4 and FMS-8) and the individual IntelliVue measurement modules.

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More Product Details

Catalog Number

865241

Brand Name

PHILIPS IntelliVue MX700 patient monitor

Version/Model Number

IntelliVue Patient Monitor MX700

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

MHX

Product Code Name

MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)

Device Record Status

Public Device Record Key

abc0b172-fff7-42a4-8883-9592e23758b9

Public Version Date

August 15, 2022

Public Version Number

9

DI Record Publish Date

September 26, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 6
2 A medical device with a moderate to high risk that requires special controls. 209