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"DORNIER" orthopedic seismometer - Taiwan Registration 07356344c2fb49383f7a9748e287d7e7

Access comprehensive regulatory information for "DORNIER" orthopedic seismometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 07356344c2fb49383f7a9748e287d7e7 and manufactured by DORNIER MEDTECH SYSTEMS GMBH. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..

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07356344c2fb49383f7a9748e287d7e7
Registration Details
Taiwan FDA Registration: 07356344c2fb49383f7a9748e287d7e7
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Device Details

"DORNIER" orthopedic seismometer
TW: โ€œๅคšๅฐผ็ˆพโ€้ชจ็ง‘้œ‡ๆณขๅ„€
Risk Class 3
Cancelled

Registration Details

07356344c2fb49383f7a9748e287d7e7

DHA00602183209

Company Information

Germany

Product Details

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

N Orthopedics

N.0001 ้ชจ็ง‘็”จ้ซ”ๅค–้œ‡ๆณข็ณป็ตฑ

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". input

Dates and Status

Dec 10, 2010

Dec 10, 2015

Jul 31, 2018

Cancellation Information

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