Taiwan FDA registration bb4d6af3e5643fa11ea8294a11093826
“Brainlab” iPlan Treatment Planning system
TW: “博醫來”電腦治療計畫系統
Taiwan·Risk Class 2·MD·BRAINLAB AG·Registered Apr 08, 2019 – Apr 08, 2024ExpiredRegistration details
- Analysis ID
- bb4d6af3e5643fa11ea8294a11093826
- License Form
- Ministry of Health Medical Device Import No. 032556
- Customs Code
- DHA05603255602
Company information
- Manufacturer
- BRAINLAB AG
- Manufacturer Country
- Germany
- Authorized Representative
- WISDOM UNION ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P5050 Medical Charged Particle Radiotherapy System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 08, 2019
- Expiry Date
- Apr 08, 2024
About this record
Access comprehensive regulatory information for “Brainlab” iPlan Treatment Planning system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bb4d6af3e5643fa11ea8294a11093826 and manufactured by BRAINLAB AG. The authorized representative in Taiwan is WISDOM UNION ENTERPRISE CO., LTD..
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