FDA Registration Active 🇺🇸 United States

867036, IntelliVue Multi-Measurement Module MMX

Reg #: 3016701404 · FEI: 3016701404 · Expires 2025
Products
8
Proprietary Names
1
Establishment Types
1
Classifications
8

Registration Details

Registration Name
Philips North America LLC
Registration Number
3016701404
FEI Number
3016701404
Status
Active
Expiry Year
2025
Initial Importer
No
Address
1003 Corporate Lane, STE B
City
Export
State
PA
ZIP
15632
Country
US

Regulatory Submissions

510(k) Number
K181831

Owner / Operator

Firm Name
Philips Medical Systems International BV
Operator Number
1217116
Address
Veenpluis 6
City
Best
State
NL-NOTA
Postal Code
5684PC
Country
NL

Products

Device Name Product Code
Computer, Diagnostic, Pre-Programmed, Single-Function DXG
Detector And Alarm, Arrhythmia DSI
Amplifier And Signal Conditioner, Transducer Signal DRQ
Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) MHX
System, Measurement, Blood-Pressure, Non-Invasive DXN
Alarm, Blood-Pressure DSJ
Computer, Blood-Pressure DSK
Monitor, St Segment With Alarm MLD

Proprietary Names

867036, IntelliVue Multi-Measurement Module MMX

Establishment Types

Manufacture Medical Device for Another Party (Contract Manufacturer)