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“Acare”Handheld Pulse Oximeter with SPO2 Probe - Taiwan Registration 9f8882b428bd782a9c59433c0f2469fa

Access comprehensive regulatory information for “Acare”Handheld Pulse Oximeter with SPO2 Probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9f8882b428bd782a9c59433c0f2469fa and manufactured by The second factory of Zhongli Technology Co., Ltd. The authorized representative in Taiwan is ACARE TECHNOLOGY CO., LTD..

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9f8882b428bd782a9c59433c0f2469fa
Registration Details
Taiwan FDA Registration: 9f8882b428bd782a9c59433c0f2469fa
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Device Details

“Acare”Handheld Pulse Oximeter with SPO2 Probe
TW: “眾里”掌上型觸控式血氧濃度儀及其配件
Risk Class 2
MD

Registration Details

9f8882b428bd782a9c59433c0f2469fa

Ministry of Health Medical Device Manufacturing No. 007795

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E2700 Oximeter

Produced in Taiwan, China

Dates and Status

Jan 16, 2023

Jan 16, 2028