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"Schneihui" meniscus repair system - Taiwan Registration 26584c4e7076ad7eda87c4f9bf6544d3

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 26584c4e7076ad7eda87c4f9bf6544d3 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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26584c4e7076ad7eda87c4f9bf6544d3
Registration Details
Taiwan FDA Registration: 26584c4e7076ad7eda87c4f9bf6544d3
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Device Details

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

Registration Details

26584c4e7076ad7eda87c4f9bf6544d3

DHA00602300803

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order. Change efficiency, counterfeit label change: see Chinese copy of the copy. (The original approved copy of the imitation single label approved in 100.11.24 shall be recycled and invalidated).

I General, Plastic Surgery and Dermatology

I.5000 Non-absorbable polyethylene terephthalate sewing wire

Input;; Contract manufacturing

Dates and Status

Nov 11, 2011

Nov 11, 2026