Taiwan FDA registration 715f64f440763e61db9be86b5ea48131

“Gemore” Fingertip Pulse Oximeter

TW: “吉懋”指尖式脈搏血氧儀

Taiwan·Risk Class 2·MD·Jimao Technology Co., Ltd. freshwater plant·Registered May 19, 2014 – May 19, 2024Expired

Registration details

Analysis ID: 715f64f440763e61db9be86b5ea48131
License Form: Ministry of Health Medical Device Manufacturing No. 004601

Company information

Manufacturer: Jimao Technology Co., Ltd. freshwater plant
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Jimao Technology Co., Ltd. freshwater plant

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): E Cardiovascular devices
Product Type (Level 2): E2700 Oximeter
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: May 19, 2014
Expiry Date: May 19, 2024

About this record

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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