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“Acare”Pulse Oximeter - Taiwan Registration 1d1612f5c6b6f7728fc0bacad3db9ff5

Access comprehensive regulatory information for “Acare”Pulse Oximeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1d1612f5c6b6f7728fc0bacad3db9ff5 and manufactured by The second factory of Zhongli Technology Co., Ltd. The authorized representative in Taiwan is ACARE TECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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1d1612f5c6b6f7728fc0bacad3db9ff5
Registration Details
Taiwan FDA Registration: 1d1612f5c6b6f7728fc0bacad3db9ff5
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Device Details

“Acare”Pulse Oximeter
TW: “眾里”血氧濃度計
Risk Class 2
MD

Registration Details

1d1612f5c6b6f7728fc0bacad3db9ff5

Ministry of Health Medical Device Manufacturing No. 007477

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

May 31, 2022

May 31, 2027