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"Schneihui" meniscus repair system - Taiwan Registration 01d3e5ca66ea3c8a82d68f92dc04209a

Access comprehensive regulatory information for "Schneihui" meniscus repair system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 01d3e5ca66ea3c8a82d68f92dc04209a and manufactured by ArthroCare Corporation;; SMITH & NEPHEW INC. ENDOSCOPY. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including ArthroCare Corporation;; SMITH & NEPHEW INC. ENDOSCOPY, Ceterix Orthopaedics, Inc.;; SMITH & NEPHEW INC. ENDOSCOPY DIVISION, and 3 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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01d3e5ca66ea3c8a82d68f92dc04209a
Registration Details
Taiwan FDA Registration: 01d3e5ca66ea3c8a82d68f92dc04209a
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Device Details

"Schneihui" meniscus repair system
TW: "ๅฒ่€่ผ" ๅŠๆœˆๆฟไฟฎ่ฃœ็ณป็ตฑ
Risk Class 2

Registration Details

01d3e5ca66ea3c8a82d68f92dc04209a

DHA00601083708

Company Information

Product Details

I General, Plastic Surgery and Dermatology

Input;; Contract manufacturing

Dates and Status

Sep 09, 2004

Sep 09, 2029