Taiwan FDA registration 73487f153cc272eee7f3903611731f9c
“Stereotaxis” Niobe Magnetic Navigation System
TW: “斯迪奧鈦思”耐歐比磁導航系統
Taiwan·Risk Class 2·MD·Stereotaxis, Inc.·Registered Aug 19, 2015 – Aug 19, 2025ExpiredRegistration details
- Analysis ID
- 73487f153cc272eee7f3903611731f9c
- License Form
- Ministry of Health Medical Device Import No. 027600
- Customs Code
- DHA05602760001
Company information
- Manufacturer
- Stereotaxis, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- UPWARDS BIOSYSTEMS LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- The E1290 controls the catheter control system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 19, 2015
- Expiry Date
- Aug 19, 2025
About this record
Access comprehensive regulatory information for “Stereotaxis” Niobe Magnetic Navigation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 73487f153cc272eee7f3903611731f9c and manufactured by Stereotaxis, Inc.. The authorized representative in Taiwan is UPWARDS BIOSYSTEMS LTD..
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