Taiwan FDA registration 843ad63afecd48b75cdcfee469278c2a
Akkiscan Zee+ Blood Glucose Monitoring System
TW: “衡欣”阿司吉血糖測試系統
Taiwan·Risk Class 2·MD·Hengxin Medical Equipment Co., Ltd·Registered Jun 13, 2016 – Oct 28, 2020CancelledRegistration details
- Analysis ID
- 843ad63afecd48b75cdcfee469278c2a
- License Form
- Ministry of Health Medical Device Manufacturing No. 005181
Company information
- Manufacturer
- Hengxin Medical Equipment Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Hengxin Medical Equipment Co., Ltd
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1345 Glucose Test System
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jun 13, 2016
- Expiry Date
- Oct 28, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Akkiscan Zee+ Blood Glucose Monitoring System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 843ad63afecd48b75cdcfee469278c2a and manufactured by Hengxin Medical Equipment Co., Ltd. The authorized representative in Taiwan is Hengxin Medical Equipment Co., Ltd.
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