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"Schneihui" external fixation system - Taiwan Registration 36c61f068896049d26634cec5f444424

Access comprehensive regulatory information for "Schneihui" external fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 36c61f068896049d26634cec5f444424 and manufactured by Smith & Nephew, Inc.. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Smith & Nephew, Inc., and 1 recent registrations in the same category. 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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36c61f068896049d26634cec5f444424
Registration Details
Taiwan FDA Registration: 36c61f068896049d26634cec5f444424
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Device Details

"Schneihui" external fixation system
TW: โ€œๅฒ่€่ผโ€ๅค–ๅ›บๅฎš็ณป็ตฑ
Risk Class 2

Registration Details

36c61f068896049d26634cec5f444424

DHA00601776100

Company Information

Product Details

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

N Orthopedics

N.3030 Single or multiple metallic bone fixation devices and accessories

import

Dates and Status

Feb 06, 2007

Feb 06, 2027

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