Pure Global

Automated External Defibrillator - SFDA Registration ME0000000143SFDAA00030

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 Database
Powered by Pure Global AI
SFDA Official Data
Class IIb
ME0000000143SFDAA00030
Automated External Defibrillator
SFDA Registration: ME0000000143SFDAA00030
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product 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
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

[]