"Axon" electronic proximity therapy system
Taiwan·Risk Class 2·XOFT, INC.·Registered Apr 24, 2012 – Apr 24, 2017Cancelled- Analysis ID
- d1b71735972c18f327dd8c7826fa0b0b
- Customs Code
- DHAS0602332204
- Manufacturer
- XOFT, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Meide Medical Devices Co., Ltd
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.5900 X光放射線治療系統
- Import Information
- Input;; Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.
- Registration Date
- Apr 24, 2012
- Expiry Date
- Apr 24, 2017
- Cancellation Date
- Dec 20, 2019
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for "Axon" electronic proximity therapy system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d1b71735972c18f327dd8c7826fa0b0b and manufactured by XOFT, INC.. The authorized representative in Taiwan is Meide Medical Devices Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Xoft, a subsidiary of iCAD, and 1 recent registrations in the same category. 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.