Taiwan FDA registration 06d409fb08d95e933219682608a1f202
“DailyCare” Handheld ECG Monitor
TW: “達楷”隨身簡易型心電圖機
Taiwan·Risk Class 2·MD·Dakai Biomedical Technology Co., Ltd·Registered Dec 01, 2015 – Dec 01, 2020CancelledRegistration details
- Analysis ID
- 06d409fb08d95e933219682608a1f202
- License Form
- Ministry of Health Medical Device Manufacturing No. 005209
Company information
- Manufacturer
- Dakai Biomedical Technology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Dakai Biomedical Technology Co., Ltd
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E2340 ECG Scanner
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Dec 01, 2015
- Expiry Date
- Dec 01, 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 “DailyCare” Handheld ECG Monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 06d409fb08d95e933219682608a1f202 and manufactured by Dakai Biomedical Technology Co., Ltd. The authorized representative in Taiwan is Dakai Biomedical Technology Co., Ltd.
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