"Stryker" clinical sample (unsterilized)
Taiwan·Risk Class 1·ORTHOVITA INC.;; STRYKER LEIBINGER GMBH & CO. KG·Registered Apr 18, 2012 – Apr 18, 2022Cancelled- Analysis ID
- ea65abc9e5ff0b86dc99526e81658baa
- Customs Code
- DHA04401160907
- Manufacturer
- ORTHOVITA INC.;; STRYKER LEIBINGER GMBH & CO. KG
- Manufacturer Country
- United States;;Germany
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
- Intended Use
- Limited to the first level identification range of the "clinical use model (N.4800)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4800 Sample plate for clinical use
- Import Information
- import
- Registration Date
- Apr 18, 2012
- Expiry Date
- Apr 18, 2022
- Cancellation Date
- Apr 12, 2024
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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 ea65abc9e5ff0b86dc99526e81658baa and manufactured by ORTHOVITA INC.;; STRYKER LEIBINGER GMBH & CO. KG. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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.