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"DORNIER" bone shock wave therapy device - Taiwan Registration f6db316d54119061c9d59933b51cd6b4

Access comprehensive regulatory information for "DORNIER" bone shock wave therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number f6db316d54119061c9d59933b51cd6b4 and manufactured by DORNIER MEDTECH SYSTEMS GMBH;;DORNIER MEDTECH GMBH. The authorized representative in Taiwan is VICTORY EIGHT ENTERPRISE CO., LTD..

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f6db316d54119061c9d59933b51cd6b4
Registration Details
Taiwan FDA Registration: f6db316d54119061c9d59933b51cd6b4
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Device Details

"DORNIER" bone shock wave therapy device
TW: โ€œๅคšๅฐผ็ˆพโ€้ชจ้œ‡ๆณขๆฒป็™‚ๅ„€
Risk Class 3
Cancelled

Registration Details

f6db316d54119061c9d59933b51cd6b4

DHA05602867202

Company Information

Product Details

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

N Orthopedics

N.0001 ้ชจ็ง‘็”จ้ซ”ๅค–้œ‡ๆณข็ณป็ตฑ

import

Dates and Status

Jun 24, 2016

Jun 24, 2021

Jun 15, 2023

Cancellation Information

Logged out

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