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“XOFT” Axxent Surface Applicator - Taiwan Registration 2a9cdc5afd7d897bf74aaf29a4dcd2db

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.

This page provides complete technical specifications, regulatory compliance details. 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.

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2a9cdc5afd7d897bf74aaf29a4dcd2db
Registration Details
Taiwan FDA Registration: 2a9cdc5afd7d897bf74aaf29a4dcd2db
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Device Details

“XOFT” Axxent Surface Applicator
TW: “艾克孚”艾克生表面發射器
Risk Class 2
MD

Registration Details

2a9cdc5afd7d897bf74aaf29a4dcd2db

Ministry of Health Medical Device Import No. 025447

DHA05602544706

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

P Devices for radiology

P5900 X-ray radiotherapy system

Imported from abroad

Dates and Status

Nov 01, 2013

Nov 01, 2028