Taiwan FDA registration 2a9cdc5afd7d897bf74aaf29a4dcd2db
“XOFT” Axxent Surface Applicator
TW: “艾克孚”艾克生表面發射器
Taiwan·Risk Class 2·MD·XOFT, A SUBSIDIARY OF ICAD·Registered Nov 01, 2013 – Nov 01, 2028ActiveRegistration details
- Analysis ID
- 2a9cdc5afd7d897bf74aaf29a4dcd2db
- License Form
- Ministry of Health Medical Device Import No. 025447
- Customs Code
- DHA05602544706
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
- Nov 01, 2013
- Expiry Date
- Nov 01, 2028
About this record
Access comprehensive regulatory information for “XOFT” Axxent Surface Applicator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2a9cdc5afd7d897bf74aaf29a4dcd2db and manufactured by XOFT, A SUBSIDIARY OF ICAD. The authorized representative in Taiwan is Meide Medical Devices Co., Ltd.
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