Taiwan FDA registration 01d3e5ca66ea3c8a82d68f92dc04209a

"Schneihui" meniscus repair system

TW: "史耐輝" 半月板修補系統
Taiwan flagTaiwan·Risk Class 2·ArthroCare Corporation;; SMITH & NEPHEW INC. ENDOSCOPY·Registered Sep 09, 2004 – Sep 09, 2029Active
Registration details
Analysis ID
01d3e5ca66ea3c8a82d68f92dc04209a
Customs Code
DHA00601083708
Company information
Manufacturer Country
Costa Rica;;United States
Product details
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Import Information
Input;; Contract manufacturing
Dates and status
Registration Date
Sep 09, 2004
Expiry Date
Sep 09, 2029
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About this record

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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