Taiwan FDA registration 976e4bff4b9233a91117d99ff50217d8
“XOFT” Axxent Cervical Applicator
TW: “艾克孚”艾克生發射器
Taiwan·Risk Class 2·MD·Xoft, a subsidiary of iCAD·Registered Jan 08, 2014 – Jan 08, 2024ExpiredRegistration details
- Analysis ID
- 976e4bff4b9233a91117d99ff50217d8
- License Form
- Ministry of Health Medical Device Import No. 025686
- Customs Code
- DHA05602568601
Company information
- Manufacturer
- Xoft, a subsidiary of iCAD
- Manufacturer Country
- United States
- Authorized Representative
- Meide Medical Devices 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)
- P5900 X-ray radiotherapy system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 08, 2014
- Expiry Date
- Jan 08, 2024
About this record
Access comprehensive regulatory information for “XOFT” Axxent Cervical Applicator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 976e4bff4b9233a91117d99ff50217d8 and manufactured by Xoft, a subsidiary of iCAD. The authorized representative in Taiwan is Meide Medical Devices Co., Ltd.
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