Taiwan FDA registration fd9b28423cf398764bbed4c1b8b3b680
"PulseCath" iVAC 2L Percutaneous Ventricular Assist Device
TW: "博斯凱" 愛韋克經皮式心室輔助裝置
Taiwan·Risk Class 3·MD·PulseCath B.V.·Registered Oct 21, 2022 – Oct 21, 2027ActiveRegistration details
- Analysis ID
- fd9b28423cf398764bbed4c1b8b3b680
- License Form
- Ministry of Health Medical Device Import No. 035968
- Customs Code
- DHA05603596801
Company information
- Manufacturer
- PulseCath B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- WIN CHAMP MEDICAL 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)
- E9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 21, 2022
- Expiry Date
- Oct 21, 2027
About this record
Access comprehensive regulatory information for "PulseCath" iVAC 2L Percutaneous Ventricular Assist Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number fd9b28423cf398764bbed4c1b8b3b680 and manufactured by PulseCath B.V.. The authorized representative in Taiwan is WIN CHAMP MEDICAL CO., LTD..
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