"Schneihui" meniscus repair system
Taiwan·Risk Class 2·ArthroCare Corporation;; SMITH & NEPHEW INC. ENDOSCOPY·Registered Apr 15, 2022 – Apr 15, 2027Active- Analysis ID
- 85279e1a550609a6303411568991ad76
- Customs Code
- DHA05603538605
- Manufacturer Country
- Costa Rica;;United States
- Authorized Representative
- SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.)
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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
- Apr 15, 2022
- Expiry Date
- Apr 15, 2027
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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 85279e1a550609a6303411568991ad76 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.