Taiwan FDA registration 867cfdb05a2bf72da1a7cd1b8a00047a
"Colini" internal fistula duct
TW: 〝可利尼〞內瘻導管
Taiwan·Risk Class 2·CREATE MEDICCO., LTD. HOKKAIDO PLANT·Registered Jun 07, 2005 – Jun 07, 2025ExpiredRegistration details
- Analysis ID
- 867cfdb05a2bf72da1a7cd1b8a00047a
- Customs Code
- DHA00601136906
Company information
- Manufacturer
- CREATE MEDICCO., LTD. HOKKAIDO PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- CHINA HOSMED INTERNATIONAL INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- import
Dates and status
- Registration Date
- Jun 07, 2005
- Expiry Date
- Jun 07, 2025
About this record
Access comprehensive regulatory information for "Colini" internal fistula duct in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 867cfdb05a2bf72da1a7cd1b8a00047a and manufactured by CREATE MEDICCO., LTD. HOKKAIDO PLANT. The authorized representative in Taiwan is CHINA HOSMED INTERNATIONAL INC..
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