"Stryker" clinical sample (unsterilized)
Taiwan·Risk Class 1·K2M, INC.·Registered Oct 05, 2023 – Oct 05, 2028Active- Analysis ID
- 64c6b781a381e913f6ef94c937beff2d
- Customs Code
- DHA09402326803
- Manufacturer
- K2M, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Stryker (Far East) Co., Ltd. Taiwan Branch
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Clinical Use Model (N.4800) First Level Identification Range".
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4800 Sample plate for clinical use
- Import Information
- Input;; QMS/QSD
- Registration Date
- Oct 05, 2023
- Expiry Date
- Oct 05, 2028
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Access comprehensive regulatory information for "Stryker" clinical sample (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 64c6b781a381e913f6ef94c937beff2d and manufactured by K2M, INC.. The authorized representative in Taiwan is Stryker (Far East) Co., Ltd. Taiwan Branch.
This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including STRYKER GMBH, LISI MEDICAL ORTHOPAEDICS;; HOWMEDICA OSTEONICS CORP., and 4 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.