FDA Registration
Active
🇩🇪 Germany
867033, IntelliVue Patient Monitor MX100
Reg #: 9610816
·
FEI: 3002807167
·
Expires 2025
Products
8
Proprietary Names
6
Establishment Types
3
Classifications
8
Registration Details
- Registration Name
- Philips Medizin Systeme Boeblingen GmbH
- Registration Number
- 9610816
- FEI Number
- 3002807167
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- HEWLETT-PACKARD STRASSE 2
- City
- BOEBLINGEN Baden-Wurttemberg
- Country
- DE
Regulatory Submissions
- 510(k) Number
- K171801
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
US Agent
- Business Name
- Philips
- Contact Name
- Deborah Currlin
- Address
- 222 Jacobs Street
- City
- Cambridge
- State
- MA
- ZIP
- 02141
- Country
- US
- [email protected]
- Phone
- 858 9452753
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Continuous Measurement Thermometer | FLL | Class 2 | General Hospital | No | 2017-10-17 |
| Monitor, St Segment With Alarm | MLD | Class 2 | Cardiovascular | No | 2017-10-17 |
| Detector And Alarm, Arrhythmia | DSI | Class 2 | Cardiovascular | No | 2017-10-17 |
| Alarm, Blood-Pressure | DSJ | Class 2 | Cardiovascular | No | 2017-10-17 |
| Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) | MHX | Class 2 | Cardiovascular | No | 2017-10-17 |
| Oximeter | DQA | Class 2 | Cardiovascular | No | 2017-10-17 |
| Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm) | DRT | Class 2 | Cardiovascular | No | 2017-10-17 |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | Class 2 | Cardiovascular | No | 2017-10-17 |
Proprietary Names
867033, IntelliVue Patient Monitor MX100
453564588501, Transpac IV Dual IBP Cable
867039, IntelliVue Hemodynamic Extension
867030, IntelliVue Multi-Measurement Module X3
867043, IntelliVue Dock
989803199741, Dual IBP Adapter
Establishment Types
Complaint File Establishment per 21 CFR 820.198
Develop Specifications But Do Not Manufacture At This Facility
Manufacture Medical Device