Taiwan FDA registration 4c8cf6ed5e7532dafe995cbf783be8d3
"Alcon" Ruida limb equipment (unsterilized)
TW: “愛樂康”瑞達肢體裝具（未滅菌）
Taiwan·Risk Class 1·ALCARE CO., LTD., CHIBA FACTORY WEST·Registered Mar 26, 2007 – Mar 26, 2022CancelledRegistration details
- Analysis ID
- 4c8cf6ed5e7532dafe995cbf783be8d3
- Customs Code
- DHA04400569909
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 first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3475 Limb fittings
- Import Information
- import
Dates and status
- Registration Date
- Mar 26, 2007
- Expiry Date
- Mar 26, 2022
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Alcon" Ruida limb equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4c8cf6ed5e7532dafe995cbf783be8d3 and manufactured by ALCARE CO., LTD., CHIBA FACTORY WEST. The authorized representative in Taiwan is HORIZON INSTRUMENTS CO. ,LTD..
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