Taiwan FDA registration 7a2c013e0e365be8948f096156290752
"Elecon" wound drainage device (sterilization)
TW: “愛樂康”傷口引流裝置(滅菌)
Taiwan·Risk Class 1·ALCARE CO., LTD., CHIBA FACTORY WEST·Registered Oct 14, 2010 – Oct 14, 2020CancelledRegistration details
- Analysis ID
- 7a2c013e0e365be8948f096156290752
- Customs Code
- DHA04400937503
Company information
- Manufacturer
- ALCARE CO., LTD., CHIBA FACTORY WEST
- Manufacturer Country
- Japan
- Authorized Representative
- HORIZON INSTRUMENTS CO. ,LTD.
Product details
- Intended Use
- Limited to the scope of Grade 1 identification of "Introduction/Drainage Catheters and Their Accessories (I.4200)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4200 Incoming/Drainage Tubes and Accessories
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Oct 14, 2010
- Expiry Date
- Oct 14, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Elecon" wound drainage device (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7a2c013e0e365be8948f096156290752 and manufactured by ALCARE CO., LTD., CHIBA FACTORY WEST. The authorized representative in Taiwan is HORIZON INSTRUMENTS CO. ,LTD..
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