"Schneihui" laparoscopic instrument
- Analysis ID
- b90a83a75cdf9ace8b03d0e2f764af58
- Customs Code
- DHA00601794201
- Manufacturer
- SMITH & NEPHEW INC. ENDOSCOPY DIVISION
- Manufacturer Country
- United States
- Authorized Representative
- SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.)
- 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
- Mar 15, 2007
- Expiry Date
- Mar 15, 2017
- Cancellation Date
- Nov 15, 2019
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Schneihui" laparoscopic instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b90a83a75cdf9ace8b03d0e2f764af58 and manufactured by SMITH & NEPHEW INC. ENDOSCOPY DIVISION. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SMITH & NEPHEW INC. ENDOSCOPY DIVISION, 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.