Taiwan FDA registration 4aceac736e584d6b935fc97207696169
"Schneihui" articular cartilage probe
TW: “史耐輝”關節軟骨探針
Taiwan·Risk Class 2·SMITH & NEPHEW INC., ENDOSCOPY DIVISION·Registered Mar 04, 2008 – Mar 04, 2018CancelledRegistration details
- Analysis ID
- 4aceac736e584d6b935fc97207696169
- Customs Code
- DHA00601861606
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)
- I General, Plastic Surgery and Dermatology
- Import Information
- import
Dates and status
- Registration Date
- Mar 04, 2008
- Expiry Date
- Mar 04, 2018
- Cancellation Date
- Nov 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Schneihui" articular cartilage probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4aceac736e584d6b935fc97207696169 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