Taiwan FDA registration f50d92e7b5f6ddfa009db081650f8428
"Overflowing" limb equipment (unsterilized)
TW: "溋溢" 肢體裝具 (未滅菌)
Taiwan·Risk Class 1·BONE METAL CO., LTD.·Registered Apr 25, 2016 – Apr 25, 2026CancelledRegistration details
- Analysis ID
- f50d92e7b5f6ddfa009db081650f8428
Company information
- Manufacturer
- BONE METAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BONE METAL 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
- Domestic
Dates and status
- Registration Date
- Apr 25, 2016
- Expiry Date
- Apr 25, 2026
- 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 "Overflowing" 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 f50d92e7b5f6ddfa009db081650f8428 and manufactured by BONE METAL CO., LTD.. The authorized representative in Taiwan is BONE METAL CO., LTD..
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