Saudi Arabia SFDA registration ME0000000143SFDAA00033
Electrocardiograph
Product information
Cardiac function monitor
Product use
Intended to acquire analyze display store and record the patient’s electrocardiographic information for clinical diagnosis and
study
Device classification
- Risk Class
- Class IIa
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000000143SFDAA00033
- Authorization ID
- MDMA-1-2017-1769
- Status
- Active
- Expire Date
- May 25, 2027
Manufacturer
- Manufacturer Name
- Shenzhen Mindray Bio-medical Electronics Co., Ltd.
Model information
- Model ID(s)
- BeneHeart R3 BeneHeart R12
Product accessories
[]
About this record
Access comprehensive regulatory information for Electrocardiograph in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIa device is registered with Saudi Arabia SFDA under registration number ME0000000143SFDAA00033 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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