"Schneihui" meniscus repair system
Taiwan·Risk Class 2·ArthroCare Corporation;; SMITH & NEPHEW INC. ENDOSCOPY·Registered Nov 11, 2011 – Nov 11, 2026Active- Analysis ID
- 26584c4e7076ad7eda87c4f9bf6544d3
- Customs Code
- DHA00602300803
- Manufacturer Country
- Costa Rica;;United States
- Authorized Representative
- SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.)
- Intended Use
- 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).
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.5000 Non-absorbable polyethylene terephthalate sewing wire
- Import Information
- Input;; Contract manufacturing
- Registration Date
- Nov 11, 2011
- Expiry Date
- Nov 11, 2026
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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.