Taiwan FDA registration fdfd5c13abbcb83a7462de30a6590827
“HeartSine” Samaritan PAD
TW: “艾心”史麥特自動體外去顫器
Taiwan·Risk Class 3·MD·HeartSine Technologies Ltd.·Registered Jun 27, 2016 – Jun 27, 2021CancelledRegistration details
- Analysis ID
- fdfd5c13abbcb83a7462de30a6590827
- License Form
- Ministry of Health Medical Device Import No. 028616
- Customs Code
- DHA05602861605
Company information
- Manufacturer
- HeartSine Technologies Ltd.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EVERMEDICAL COMPANY LTD.
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E5310 Automated External Defibrillator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 27, 2016
- Expiry Date
- Jun 27, 2021
- Cancellation Date
- Aug 23, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “HeartSine” Samaritan PAD in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number fdfd5c13abbcb83a7462de30a6590827 and manufactured by HeartSine Technologies Ltd.. The authorized representative in Taiwan is EVERMEDICAL COMPANY 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.
Free DatabasePowered by Pure Global AI89,000+ Devices