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“XOFT” Axxent Cervical Applicator - Taiwan Registration 976e4bff4b9233a91117d99ff50217d8

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.

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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976e4bff4b9233a91117d99ff50217d8
Registration Details
Taiwan FDA Registration: 976e4bff4b9233a91117d99ff50217d8
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Device Details

“XOFT” Axxent Cervical Applicator
TW: “艾克孚”艾克生發射器
Risk Class 2
MD

Registration Details

976e4bff4b9233a91117d99ff50217d8

Ministry of Health Medical Device Import No. 025686

DHA05602568601

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

Jan 08, 2014

Jan 08, 2024