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"Shimadzu" X-ray diagnostic system - Taiwan Registration 44810b5fe7759f6cb96515c1a3ec6a05

Access comprehensive regulatory information for "Shimadzu" X-ray diagnostic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 44810b5fe7759f6cb96515c1a3ec6a05 and manufactured by SHIMADZU CORPORATION, SANJO FACTORY. The authorized representative in Taiwan is SAN KANG INSTRUMENTS 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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44810b5fe7759f6cb96515c1a3ec6a05
Registration Details
Taiwan FDA Registration: 44810b5fe7759f6cb96515c1a3ec6a05
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Device Details

"Shimadzu" X-ray diagnostic system
TW: โ€œๅณถๆดฅโ€Xๅ…‰้€่ฆ–่จบๆ–ท็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

44810b5fe7759f6cb96515c1a3ec6a05

DHAS0602021208

Company Information

Product Details

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

P Radiology Science

P.1660 ้ž้€่ฆ–Xๅ…‰ๅฝฑๅƒๅขžๆ„Ÿ็ฎก

Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input

Dates and Status

Sep 30, 2009

Sep 30, 2019

Jun 16, 2022

Cancellation Information

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