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Patient Monitor - SFDA Registration ME0000000143SFDAA00204

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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SFDA Official Data
Class IIb
ME0000000143SFDAA00204
Patient Monitor
SFDA Registration: ME0000000143SFDAA00204
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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
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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