Identity
- Trade Name
- IntelliVue Patient Monitor MX800 EUDAMEDIntelliVue MX800 patient monitor FDA UDI
- Generic Name
- General-purpose multi-parameter bedside monitor FDA UDI
- Device Name
- MX700/800 EUDAMEDThe IntelliVue MX800 patient monitor is operated primarily via touch screen. It has an integrated 19" TFT widescreen touch display and is compatible with the IntelliVue Multi Measurement Module (M3001A)/ IntelliVue X2 (M3002A)/ all Multi-Measurement Module Extensions/IntelliVue MMX (867036)/ IntelliVue X3 (867030)/ the Flexible Module Server (M8048A) and the individual IntelliVue measurement modules. FDA UDI
- Model / Reference
- 865240 EUDAMEDIntelliVue Patient Monitor MX800 FDA UDI
- Description
- The IntelliVue MX800 patient monitor is operated primarily via touch screen. It has an integrated 19" TFT widescreen touch display and is compatible with the IntelliVue Multi Measurement Module (M3001A)/ IntelliVue X2 (M3002A)/ all Multi-Measurement Module Extensions/IntelliVue MMX (867036)/ IntelliVue X3 (867030)/ the Flexible Module Server (M8048A) and the individual IntelliVue measurement modules. FDA UDI
Identifiers
- Catalog Number
- 865240 FDA UDI
- Primary DI / UDI-DI
- 00884838020733 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00884838020733 EUDAMED
- FDA Product Code
- MHX FDA UDI
- EMDN Code
- Z1203020201 MULTI–PARAMETER PATIENT BEDSIDE MONITORS EUDAMED
- GMDN Term
- General-purpose multi-parameter bedside monitor FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 870.1025 FDA UDI
- Market of Registration
- Austria EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
Yes
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
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
IntelliVue Patient Monitor MX800 by Philips Medizin Systeme Böblingen GmbH — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00884838020733 | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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Manufacturer
- Manufacturer
- Philips Medizin Systeme Böblingen GmbH
- EUDAMED SRN
- DE-MF-000006026
Sources (2)
- EUDAMED fc02e4c5-cba1-4a8d-915e-a134918a8b11 61 fields · synced Jun 6, 2026
- FDA UDI e765c8d2-3306-4f89-bcce-f019a1f0f840 36 fields · synced May 29, 2026