"Stryker" medical light source machine
Taiwan·Risk Class 2·STRYKER ENDOSCOPY·Registered May 13, 2005 – May 13, 2020Cancelled- Analysis ID
- a9442465b88f509129f2ae70ac39c8ae
- Customs Code
- DHA00601131700
- 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)
- I General, Plastic Surgery and Dermatology
- Import Information
- import
- Registration Date
- May 13, 2005
- Expiry Date
- May 13, 2020
- Cancellation Date
- Jun 18, 2020
- Status
- Logged out
- Reason
- 自請註銷
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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 a9442465b88f509129f2ae70ac39c8ae 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.