Taiwan FDA registration 25424d559f5540c19da9d3570cfe6265
AndoCor Aortic Root Cannulae
TW: 恩多寇主動脈根部導管
Taiwan·Risk Class 2·MD·ANDOCOR NV·Registered Apr 25, 2018 – Apr 25, 2023ExpiredRegistration details
- Analysis ID
- 25424d559f5540c19da9d3570cfe6265
- License Form
- Ministry of Health Medical Device Import No. 030819
- Customs Code
- DHA05603081901
Company information
- Manufacturer
- ANDOCOR NV
- Manufacturer Country
- Belgium
- Authorized Representative
- LEIN YIH MEDICAL CO.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E4210 Vascular catheters, cannula and tubes for cardiopulmonary vascular bypass
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 25, 2018
- Expiry Date
- Apr 25, 2023
About this record
Access comprehensive regulatory information for AndoCor Aortic Root Cannulae in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 25424d559f5540c19da9d3570cfe6265 and manufactured by ANDOCOR NV. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..
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