Taiwan FDA registration cfa89351f1b1f730e4b1bf53557f6467
AndoCor Ostial Perfusion Cannula
TW: 恩多寇冠狀動脈口灌注導管
Taiwan·Risk Class 2·MD·ANDOCOR NV·Registered Apr 16, 2018 – Apr 16, 2023ExpiredRegistration details
- Analysis ID
- cfa89351f1b1f730e4b1bf53557f6467
- License Form
- Ministry of Health Medical Device Import No. 030808
- Customs Code
- DHA05603080806
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 16, 2018
- Expiry Date
- Apr 16, 2023
About this record
Access comprehensive regulatory information for AndoCor Ostial Perfusion Cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cfa89351f1b1f730e4b1bf53557f6467 and manufactured by ANDOCOR NV. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..
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