Saudi Arabia SFDA registration ME0000000143SFDAA00030
Automated External Defibrillator
Saudi Arabia·MD·Shenzhen Mindray Bio-medical Electronics Co., Ltd.·Class IIbActiveProduct information
Defibrillator/monitor
Product use
The equipment is intended for external defibrillation internal defibrillation synchronized cardioversion and semi-automatic defibrillation (AED). It can also be used for non-invasive external pacing as well as ECG SpO2 PR NIBP, CO2 IBP and Temp monitoring
Device classification
- Risk Class
- Class IIb
- Product Category
- MD
- Product Type
- MD
Registration information
- Registration ID
- ME0000000143SFDAA00030
- Authorization ID
- MDMA-1-2019-2907
- Status
- Active
- Expire Date
- May 26, 2024
Manufacturer
- Manufacturer Name
- Shenzhen Mindray Bio-medical Electronics Co., Ltd.
Model information
- Model ID(s)
- BeneHeart D1 BeneHeart C1 Fully Automatic BeneHeart C1A Fully Automatic BeneHeart C2 Fully Automatic BeneHeart C2A Fully Automatic BeneHeart C1 BeneHeart C1A BeneHeart C2 BeneHeart C2A
Product accessories
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About this record
Access comprehensive regulatory information for Automated External Defibrillator 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 ME0000000143SFDAA00030 and manufactured by Shenzhen Mindray Bio-medical Electronics Co., Ltd..
This page provides complete registration details including product category (MD), 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.
Free DatabasePowered by Pure Global AISFDA Official DataClass IIb