"Stryker" medical light source machine
Taiwan·Risk Class 2·STRYKER ENDOSCOPY·Registered Jan 18, 2010 – Jan 18, 2025Expired- Analysis ID
- 5ae6aa354108f05759cbd98526974013
- Customs Code
- DHA00602052903
- Manufacturer
- STRYKER ENDOSCOPY
- Manufacturer Country
- United States
- 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)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
- Registration Date
- Jan 18, 2010
- Expiry Date
- Jan 18, 2025
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Access comprehensive regulatory information for "Stryker" medical light source machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5ae6aa354108f05759cbd98526974013 and manufactured by STRYKER ENDOSCOPY. 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 ENDOSCOPY, and 2 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.