Taiwan FDA registration 71c8d636e5fb062425dbac20fb13307e
"Baijie" finger pulse oximeter
TW: “百捷”手指型脈搏血氧儀
Taiwan·Risk Class 2·Baichen Technology Co., Ltd·Registered Dec 01, 2022 – Dec 01, 2027ActiveRegistration details
- Analysis ID
- 71c8d636e5fb062425dbac20fb13307e
Company information
- Manufacturer
- Baichen Technology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- VIA-TECH BIOMEDICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.2700.
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Dec 01, 2022
- Expiry Date
- Dec 01, 2027
About this record
Access comprehensive regulatory information for "Baijie" finger 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 71c8d636e5fb062425dbac20fb13307e and manufactured by Baichen Technology Co., Ltd. The authorized representative in Taiwan is VIA-TECH BIOMEDICAL CO., LTD..
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