Taiwan FDA registration ede2c86f227ef6beb05b4f7a0982b565
“OrthoDevelopment” Vusion OS System
TW: “奧森迪威”腰椎間盤融合器
Taiwan·Risk Class 2·MD·ORTHO DEVELOPMENT CORPORATION·Registered Apr 13, 2016 – Apr 13, 2021CancelledRegistration details
- Analysis ID
- ede2c86f227ef6beb05b4f7a0982b565
- License Form
- Ministry of Health Medical Device Import No. 028372
- Customs Code
- DHA05602837203
Company information
- Manufacturer
- ORTHO DEVELOPMENT CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Huixing Co., Ltd
Product details
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3080 Interbody fusion device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 13, 2016
- Expiry Date
- Apr 13, 2021
- Cancellation Date
- Aug 09, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “OrthoDevelopment” Vusion OS System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ede2c86f227ef6beb05b4f7a0982b565 and manufactured by ORTHO DEVELOPMENT CORPORATION. The authorized representative in Taiwan is Huixing Co., Ltd.
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