Taiwan FDA registration 2a1b0ad4ed0d3a3eaa2e2567b34372fa
"Xenex" Meidex femoral arteriovenous catheter
TW: “賽耐司”美德思股動靜脈導管
Taiwan·Risk Class 2·Xenios AG·Registered Jan 18, 2008 – Jan 18, 2028ActiveRegistration details
- Analysis ID
- 2a1b0ad4ed0d3a3eaa2e2567b34372fa
- Customs Code
- DHA00601855308
Company information
- Manufacturer
- Xenios AG
- Manufacturer Country
- Germany
- Authorized Representative
- HSIN TUNG MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Jan 18, 2008
- Expiry Date
- Jan 18, 2028
About this record
Access comprehensive regulatory information for "Xenex" Meidex femoral arteriovenous catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2a1b0ad4ed0d3a3eaa2e2567b34372fa and manufactured by Xenios AG. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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