Taiwan FDA registration a247b423515d938563936da387b1580b
“Acare” Finger Type Pulse Oximeter
TW: “眾里” 血氧濃度計
Taiwan·Risk Class 2·MD·The second factory of Zhongli Technology Co., Ltd·Registered Mar 31, 2023 – Mar 31, 2028ActiveRegistration details
- Analysis ID
- a247b423515d938563936da387b1580b
- License Form
- Ministry of Health Medical Device Manufacturing No. 007838
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ACARE TECHNOLOGY 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)
- E2700 Oximeter
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 31, 2023
- Expiry Date
- Mar 31, 2028
About this record
Access comprehensive regulatory information for “Acare” Finger Type 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 a247b423515d938563936da387b1580b and manufactured by The second factory of Zhongli Technology Co., Ltd. The authorized representative in Taiwan is ACARE TECHNOLOGY CO., LTD..
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