Taiwan FDA registration 448ead39f87ef9feed860a06c775353a
“OrthoDevelopment” Vusion System (CS Plus)
TW: “奧森迪威”頸椎間盤融合器
Taiwan·Risk Class 2·MD·ORTHO DEVELOPMENT CORPORATION·Registered Jul 07, 2015 – Jul 07, 2020CancelledRegistration details
- Analysis ID
- 448ead39f87ef9feed860a06c775353a
- License Form
- Ministry of Health Medical Device Import No. 027491
- Customs Code
- DHA05602749106
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
- Jul 07, 2015
- Expiry Date
- Jul 07, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for “OrthoDevelopment” Vusion System (CS Plus) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 448ead39f87ef9feed860a06c775353a and manufactured by ORTHO DEVELOPMENT CORPORATION. The authorized representative in Taiwan is Huixing Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices