Taiwan FDA registration a23790a9111874c836ed7bd336623569
"Schneihui" Argo cable system
TW: "史耐輝"雅歌鋼索系統
Taiwan·Risk Class 2·Made (部分製程) in MALAYSIA;; Smith & Nephew, Inc.·Registered Mar 02, 2006 – Mar 02, 2026ExpiredRegistration details
- Analysis ID
- a23790a9111874c836ed7bd336623569
- Customs Code
- DHA00601406705
Company information
- Manufacturer
- Made (部分製程) in MALAYSIA;; Smith & Nephew, Inc.
- Manufacturer Country
- United States;;Malaysia
- Authorized Representative
- SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Import Information
- import
Dates and status
- Registration Date
- Mar 02, 2006
- Expiry Date
- Mar 02, 2026
About this record
Access comprehensive regulatory information for "Schneihui" Argo cable system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a23790a9111874c836ed7bd336623569 and manufactured by Made (部分製程) in MALAYSIA;; Smith & Nephew, Inc.. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices