Saudi Arabia SFDA registration ME0000000143SFDAA00206
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
- ME0000000143SFDAA00206
- Authorization ID
- GHTF-2017-1770
- Status
- Active
- Expire Date
- February 21, 2020
Manufacturer
- Manufacturer Name
- Shenzhen Mindray Bio-Medical Electronics Co., Ltd
Model information
- Model ID(s)
- iPM 8 // iPM 10 // iPM 12 // BeneView T5 // BeneView T9 // BeneView T6 // BeneView T8 // iMEC8 // iMEC10 // iMEC12 // BeneView T1 // iMEC15 // BeneVision N22 // BeneVision N19 // iPM 5 // iPM 6 // iPM 7 // iMEC 5 // iMEC 6 // iMEC 7 // uMEC 6 // uMEC 7 // uMEC 10 // uMEC 12 // BeneVision N12 // BeneVision N15 // BeneVision N17 // uMEC15 // uMEC15S
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 ME0000000143SFDAA00206 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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