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"Schneihui" articular cartilage probe - Taiwan Registration 4aceac736e584d6b935fc97207696169

Access comprehensive regulatory information for "Schneihui" articular cartilage probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4aceac736e584d6b935fc97207696169 and manufactured by SMITH & NEPHEW INC., ENDOSCOPY DIVISION. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).

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4aceac736e584d6b935fc97207696169
Registration Details
Taiwan FDA Registration: 4aceac736e584d6b935fc97207696169
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Device Details

"Schneihui" articular cartilage probe
TW: โ€œๅฒ่€่ผโ€้—œ็ฏ€่ปŸ้ชจๆŽข้‡
Risk Class 2
Cancelled

Registration Details

4aceac736e584d6b935fc97207696169

DHA00601861606

Company Information

Product Details

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

I General, Plastic Surgery and Dermatology

import

Dates and Status

Mar 04, 2008

Mar 04, 2018

Nov 15, 2019

Cancellation Information

Logged out

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