Taiwan FDA registration fea0848944e368311eadf64104108af0
“DailyCare” CheckMyHeart Plus(Handheld ECG monitor)
TW: “達楷”隨身簡易型心電圖機(進階版)
Registration details
- Analysis ID
- fea0848944e368311eadf64104108af0
- License Form
- Ministry of Health Medical Device Manufacturing No. 004611
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
- May 27, 2014
- Expiry Date
- May 27, 2024
- Cancellation Date
- Aug 17, 2023
About this record
Access comprehensive regulatory information for “DailyCare” CheckMyHeart Plus(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 fea0848944e368311eadf64104108af0 and manufactured by Dakai Biomedical Technology Co., Ltd. The authorized representative in Taiwan is Dakai Biomedical Technology Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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