Saudi Arabia SFDA registration ME0000000143SFDAA00204
Patient Monitor
Product information
Medical display system
Product use
The intended use of MEC-1200 is to monitor a fixed set of parameters for single adult, pediatric and neonatal patient, to display patient data and waveforms, to store patient data in a trend database, and to generate alarms and recordings.
The physiological parameters that can be monitored by MEC-1200 Patient Monitor are: ECG, Heart Rate(HR), Pulse Rate(PR), Respiration Rate(RESP), Non-invasive Blood Pressure (NIBP), Saturation of Pulse Oxygen(SpO2), Temperature (TEMP).
Device classification
- Risk Class
- Class IIb
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000000143SFDAA00204
- Authorization ID
- MDMA-1-2019-2684
- Status
- Active
- Expire Date
- May 26, 2027
Manufacturer
- Manufacturer Name
- Shenzhen Mindray Bio-medical Electronics Co., Ltd.
Model information
- Model ID(s)
- BeneVision N22 BeneVision N19 uMEC 6 uMEC 7 uMEC 10 uMEC 12 BeneVision N12 BeneVision N15 BeneVision N17 uMEC15 uMEC15S ePM 10 ePM 12 ePM 15 ePM 10M ePM 12M ePM 15M ePM 15A ePM 15MA BeneVision N1
Product accessories
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About this record
Access comprehensive regulatory information for Patient Monitor in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIb device is registered with Saudi Arabia SFDA under registration number ME0000000143SFDAA00204 and manufactured by Shenzhen Mindray Bio-medical Electronics Co., Ltd..
This page provides complete registration details including product category (Medical Device), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.
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