Taiwan FDA registration af36028334d396cc1d06bc3a01e6e8d4
"Sindis" surgical instruments
TW: 〝信迪思〞手術器械
Registration details
- Analysis ID
- af36028334d396cc1d06bc3a01e6e8d4
- Customs Code
- DHA04400204502
Company information
- Manufacturer
- SYNTHES
- Manufacturer Country
- Switzerland
- Authorized Representative
- Taiwan Sindis Medical Equipment Co., Ltd
Product details
- Intended Use
- A manual instrument used in general surgery is a non-powered, hand-held or hand-operated device used in various general surgeries.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
Dates and status
- Registration Date
- Nov 21, 2005
- Expiry Date
- Nov 21, 2010
- Cancellation Date
- Jan 21, 2013
Cancellation information
- Status
- Logged out
About this record
Access comprehensive regulatory information for "Sindis" surgical instruments in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number af36028334d396cc1d06bc3a01e6e8d4 and manufactured by SYNTHES. The authorized representative in Taiwan is Taiwan Sindis Medical Equipment Co., Ltd.
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