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“Gemore” Fingertip Pulse Oximeter - Taiwan Registration 715f64f440763e61db9be86b5ea48131

Access comprehensive regulatory information for “Gemore” Fingertip 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 715f64f440763e61db9be86b5ea48131 and manufactured by Jimao Technology Co., Ltd. freshwater plant. The authorized representative in Taiwan is Jimao Technology Co., Ltd. freshwater plant.

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715f64f440763e61db9be86b5ea48131
Registration Details
Taiwan FDA Registration: 715f64f440763e61db9be86b5ea48131
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Device Details

“Gemore” Fingertip Pulse Oximeter
TW: “吉懋”指尖式脈搏血氧儀
Risk Class 2
MD

Registration Details

715f64f440763e61db9be86b5ea48131

Ministry of Health Medical Device Manufacturing No. 004601

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular devices

E2700 Oximeter

Produced in Taiwan, China

Dates and Status

May 19, 2014

May 19, 2024