Identity
- Trade Name
- Hemodynamic Measurement Server Extension FDA UDI
- Generic Name
- Patient monitoring system module, multifunction FDA UDI
- Device Name
- Hemodynamic Measurement Server Extension works together with the IntelliVue Multi-Measurement Module (MMS), the IntelliVue X2 Multi-Measurement Module and IntelliVue MP2 Patient Monitor. The base product provides one Invasive Pressure, one Temperature and one Invasive Pressure or Temperature channel (one at a time). Optional Right Heart Cardiac Output (C.O.) and Continuous C.O. PiCCO can be selected via C-options. FDA UDI
- Model / Reference
- Hemodynamic Measurement Server Extension FDA UDI
- Description
- Hemodynamic Measurement Server Extension works together with the IntelliVue Multi-Measurement Module (MMS), the IntelliVue X2 Multi-Measurement Module and IntelliVue MP2 Patient Monitor. The base product provides one Invasive Pressure, one Temperature and one Invasive Pressure or Temperature channel (one at a time). Optional Right Heart Cardiac Output (C.O.) and Continuous C.O. PiCCO can be selected via C-options. FDA UDI
Identifiers
- Catalog Number
- 862111 FDA UDI
- Primary DI / UDI-DI
- 00884838021532 FDA UDI
- 510(k) Number
- K033444 FDA UDI
- FDA Product Code
- MHX FDA UDI
- GMDN Term
- Patient monitoring system module, multifunction FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1025 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Hemodynamic Measurement Server Extension by Philips Medizin Systeme Böblingen GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K033444 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Philips Medizin Systeme Böblingen GmbH
Sources (1)
- FDA UDI 64dce9f6-eb20-4999-953e-6b46a450a3c0 38 fields · synced May 30, 2026