Taiwan FDA registration 8a00c967b666fb4454431d3534b4b36b
“Heartcare”Balloon Guiding Catheter
TW: “心瑋醫療”封堵球囊導管
Taiwan·Risk Class 2·MD·Shanghai Heartcare Medical Technology Corporation Limited·Registered Jul 24, 2022 – Jul 24, 2027ActiveRegistration details
- Analysis ID
- 8a00c967b666fb4454431d3534b4b36b
- License Form
- Ministry of Health Medical Device Land Transport No. 001348
- Customs Code
- DHA09200134802
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 24, 2022
- Expiry Date
- Jul 24, 2027
About this record
Access comprehensive regulatory information for “Heartcare”Balloon Guiding Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8a00c967b666fb4454431d3534b4b36b and manufactured by Shanghai Heartcare Medical Technology Corporation Limited. The authorized representative in Taiwan is DR SHAO MD REGULATORY CONSULTANTS CO., LTD..
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