Taiwan FDA registration 72ea7eb8e49f364fdd6e893daa0cfa50
"Xenex" Meidex Tubing Group
TW: “賽耐司” 美德思管路組
Taiwan·Risk Class 2·Xenios AG·Registered Feb 21, 2011 – Feb 21, 2026ExpiredRegistration details
- Analysis ID
- 72ea7eb8e49f364fdd6e893daa0cfa50
- Customs Code
- DHA00602206500
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
- Product Type (Level 2)
- E.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Feb 21, 2011
- Expiry Date
- Feb 21, 2026
About this record
Access comprehensive regulatory information for "Xenex" Meidex Tubing Group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 72ea7eb8e49f364fdd6e893daa0cfa50 and manufactured by Xenios AG. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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