Taiwan FDA registration f870f7e8b36f753d4afde55eacf7df4e
SPIO Compression Orthosis (Non-Sterile)
TW: 斯比歐增壓矯具 (未滅菌)
Taiwan·Risk Class 1·MD·SPIO, Inc.·Registered Sep 07, 2018 – Sep 07, 2023CancelledRegistration details
- Analysis ID
- f870f7e8b36f753d4afde55eacf7df4e
- License Form
- Ministry of Health Medical Device Import No. 019585
- Customs Code
- DHA09401958500
Company information
- Manufacturer
- SPIO, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- Fuyu Medical Equipment Co., Ltd
Product details
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 07, 2018
- Expiry Date
- Sep 07, 2023
- Cancellation Date
- Feb 18, 2022
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for SPIO Compression Orthosis (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f870f7e8b36f753d4afde55eacf7df4e and manufactured by SPIO, Inc.. The authorized representative in Taiwan is Fuyu Medical Equipment Co., Ltd.
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