Taiwan FDA registration 23da4a68e33afa2ac2406bd0974e9562
Qinda blood circuit tube
TW: 勤達血液迴路管
Taiwan·Risk Class 3·HOSPITECH MANUFACTURING SERVICES SDN BHD·Registered Jan 31, 2008 – Jan 31, 2023ExpiredRegistration details
- Analysis ID
- 23da4a68e33afa2ac2406bd0974e9562
- Customs Code
- DHA00601857403
Company information
- Manufacturer
- HOSPITECH MANUFACTURING SERVICES SDN BHD
- Manufacturer Country
- Malaysia
- Authorized Representative
- DORA MEDICAL EQUIPMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5820 血液透析系統及其附件
- Import Information
- import
Dates and status
- Registration Date
- Jan 31, 2008
- Expiry Date
- Jan 31, 2023
About this record
Access comprehensive regulatory information for Qinda blood circuit tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 23da4a68e33afa2ac2406bd0974e9562 and manufactured by HOSPITECH MANUFACTURING SERVICES SDN BHD. The authorized representative in Taiwan is DORA MEDICAL EQUIPMENT CO., LTD..
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