Taiwan FDA registration 8212e4e351375d3dc98725cfd2893f6c
AndoCor Pericardial Sump
TW: 恩多寇心包膜抽吸管
Taiwan·Risk Class 2·MD·ANDOCOR NV·Registered Dec 22, 2018 – Dec 22, 2023ExpiredRegistration details
- Analysis ID
- 8212e4e351375d3dc98725cfd2893f6c
- License Form
- Ministry of Health Medical Device Import No. 031877
- Customs Code
- DHA05603187704
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
- Dec 22, 2018
- Expiry Date
- Dec 22, 2023
About this record
Access comprehensive regulatory information for AndoCor Pericardial Sump in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8212e4e351375d3dc98725cfd2893f6c and manufactured by ANDOCOR NV. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..
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