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Pulse Oximeter - SFDA Registration ME0000000143SFDAA00205

Access comprehensive regulatory information for Pulse Oximeter 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 ME0000000143SFDAA00205 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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Class IIb
ME0000000143SFDAA00205
Pulse Oximeter
SFDA Registration: ME0000000143SFDAA00205
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Product Information

Patient Monitor

Product Use

The PM-50 and PM-60 Pulse Oximeter is a non-invasive, spot-check, oxygen saturation and pulse rate monitor. It operates only on battery power using existing PM-50 disposable and reusable finger and ear sensors labeled for patients ranging from neonates to adults.

Device Classification
Risk Class
Class IIb
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000000143SFDAA00205
Authorization ID
GHTF-2017-0783
Status
Active
Expire Date
February 21, 2020
Model Information
Model ID(s)
PM-60
Product Accessories

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