Taiwan FDA registration 87512f869d419df85356d71c13bbf1ac
"Yanbo" fingertip pulse oximeter
TW: “雃博”指尖式脈搏血氧儀
Taiwan·Risk Class 2·Jimao Technology Co., Ltd. freshwater plant·Registered Aug 14, 2015 – May 19, 2019CancelledRegistration details
- Analysis ID
- 87512f869d419df85356d71c13bbf1ac
Company information
- Manufacturer
- Jimao Technology Co., Ltd. freshwater plant
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Wellell Inc.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.2700.
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Aug 14, 2015
- Expiry Date
- May 19, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Yanbo" 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 87512f869d419df85356d71c13bbf1ac and manufactured by Jimao Technology Co., Ltd. freshwater plant. The authorized representative in Taiwan is Wellell Inc..
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