Taiwan FDA registration 19db29a475625417fb7d3d085abc60b2
“Heartcare”Micro Catheter
TW: “心瑋醫療”微導管
Taiwan·Risk Class 2·MD·Shanghai Heartcare Medical Technology Corporation Limited·Registered Jul 10, 2022 – Jul 10, 2027ActiveRegistration details
- Analysis ID
- 19db29a475625417fb7d3d085abc60b2
- License Form
- Ministry of Health Medical Device Land Transport No. 001343
- Customs Code
- DHA09200134305
Company information
- Manufacturer Country
- China
- Authorized Representative
- DR SHAO MD REGULATORY CONSULTANTS 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)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Jul 10, 2022
- Expiry Date
- Jul 10, 2027
About this record
Access comprehensive regulatory information for “Heartcare”Micro Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 19db29a475625417fb7d3d085abc60b2 and manufactured by Shanghai Heartcare Medical Technology Corporation Limited. The authorized representative in Taiwan is DR SHAO MD REGULATORY CONSULTANTS 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.
Free DatabasePowered by Pure Global AI89,000+ Devices