"Stryker" ultrasound surgical device
Taiwan·Risk Class 2·STRYKER INSTRUMENTS;; STRYKER MEDTECH K.K.·Registered Sep 16, 2011 – Sep 16, 2026Active- Analysis ID
- 4e84d0e7f9790de23596b53ee2d5a33a
- Customs Code
- DHA00602279202
- Manufacturer
- STRYKER INSTRUMENTS;; STRYKER MEDTECH K.K.
- Manufacturer Country
- United States;;Japan
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.0003 Ultrasound surgical device
- Import Information
- import
- Registration Date
- Sep 16, 2011
- Expiry Date
- Sep 16, 2026
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Access comprehensive regulatory information for "Stryker" ultrasound surgical device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4e84d0e7f9790de23596b53ee2d5a33a and manufactured by STRYKER INSTRUMENTS;; STRYKER MEDTECH K.K.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including STRYKER LEIBINGER GMBH & CO. KG;; Stryker Instruments, and 1 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.