Taiwan FDA registration 91d91df86b6f67347fc2ab53576a9c7d
“Heartcare”Distal Access Catheter
TW: “心瑋醫療”遠端通路導管
Taiwan·Risk Class 2·MD·Shanghai Heartcare Medical Technology Corporation Limited·Registered Nov 22, 2022 – Nov 22, 2027ActiveRegistration details
- Analysis ID
- 91d91df86b6f67347fc2ab53576a9c7d
- License Form
- Ministry of Health Medical Device Land Transport No. 001399
- Customs Code
- DHA09200139906
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
- Nov 22, 2022
- Expiry Date
- Nov 22, 2027
About this record
Access comprehensive regulatory information for “Heartcare”Distal Access Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 91d91df86b6f67347fc2ab53576a9c7d 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