Taiwan FDA registration 493ab4985e7e9693c6275cacc57817f7
"Sneihui" high-resolution photography system
TW: "史耐輝"高解析攝影系統
Registration details
- Analysis ID
- 493ab4985e7e9693c6275cacc57817f7
- Customs Code
- DHA00601436806
Company information
- Manufacturer
- SMITH & NEPHEW INC., ENDOSCOPY DIVISION
- Manufacturer Country
- United States
- Authorized Representative
- SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- import
Dates and status
- Registration Date
- Apr 28, 2006
- Expiry Date
- Apr 28, 2016
- Cancellation Date
- Jun 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Sneihui" high-resolution photography system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 493ab4985e7e9693c6275cacc57817f7 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. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices