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"DORNIER" urological imaging system - Taiwan Registration bb7bdbaf7a6e2e0ac71e388cf1893b7f

Access comprehensive regulatory information for "DORNIER" urological imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bb7bdbaf7a6e2e0ac71e388cf1893b7f and manufactured by DORNIER MEDTECH SYSTEMS GMBH. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..

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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bb7bdbaf7a6e2e0ac71e388cf1893b7f
Registration Details
Taiwan FDA Registration: bb7bdbaf7a6e2e0ac71e388cf1893b7f
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Device Details

"DORNIER" urological imaging system
TW: โ€œๅคšๅฐผ็ˆพโ€ๆณŒๅฐฟ็ง‘ๅฝฑๅƒ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

bb7bdbaf7a6e2e0ac71e388cf1893b7f

DHAS5602666605

Company Information

Germany

Product Details

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

P Radiology Science

P.1730 ็…ง็›ธ้€่ฆ–Xๅ…‰็ณป็ตฑ

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

Dates and Status

Oct 31, 2014

Oct 31, 2019

Jul 15, 2022

Cancellation Information

Logged out

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