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"Dikang" X-ray system - Taiwan Registration 22fb95f8c8ffa289a94045a796062455

Access comprehensive regulatory information for "Dikang" X-ray system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 22fb95f8c8ffa289a94045a796062455 and manufactured by DK MEDICAL SYSTEMS CO., LTD.. The authorized representative in Taiwan is FONN CHANG TRADING 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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22fb95f8c8ffa289a94045a796062455
Registration Details
Taiwan FDA Registration: 22fb95f8c8ffa289a94045a796062455
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Device Details

"Dikang" X-ray system
TW: โ€œๅธๅบทโ€Xๅ…‰็ณป็ตฑ
Risk Class 2

Registration Details

22fb95f8c8ffa289a94045a796062455

DHAS5602816009

Company Information

Korea, Republic of

Product Details

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

P Radiology Science

P.1680 ๅ›บๅฎšๅผXๅ…‰็ณป็ตฑ

Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and Status

Jan 28, 2016

Jan 28, 2026