"Stryker" clinical sample (unsterilized)
Taiwan·Risk Class 1·LISI MEDICAL ORTHOPAEDICS;; HOWMEDICA OSTEONICS CORP.·Registered Aug 07, 2023 – Aug 07, 2028Active- Analysis ID
- 696845d023be21592265ca8af08151a1
- Customs Code
- DHA09402320607
- Manufacturer Country
- France;;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
- QMS/QSD;; 委託製造;; 輸入
- Registration Date
- Aug 07, 2023
- Expiry Date
- Aug 07, 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 696845d023be21592265ca8af08151a1 and manufactured by LISI MEDICAL ORTHOPAEDICS;; HOWMEDICA OSTEONICS CORP.. 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, ORTHOVITA INC.;; STRYKER LEIBINGER GMBH & CO. KG, 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.