Taiwan FDA registration 9f8882b428bd782a9c59433c0f2469fa
“Acare”Handheld Pulse Oximeter with SPO2 Probe
TW: “眾里”掌上型觸控式血氧濃度儀及其配件
Taiwan·Risk Class 2·MD·The second factory of Zhongli Technology Co., Ltd·Registered Jan 16, 2023 – Jan 16, 2028ActiveRegistration details
- Analysis ID
- 9f8882b428bd782a9c59433c0f2469fa
- License Form
- Ministry of Health Medical Device Manufacturing No. 007795
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
- Jan 16, 2023
- Expiry Date
- Jan 16, 2028
About this record
Access comprehensive regulatory information for “Acare”Handheld Pulse Oximeter with SPO2 Probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9f8882b428bd782a9c59433c0f2469fa 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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