Taiwan FDA registration 497735abc6893913257490561df56d6a
Sudamix gel (unsterilized)
TW: 舒達美凝膠(未滅菌)
Registration details
- Analysis ID
- 497735abc6893913257490561df56d6a
- Customs Code
- DHA04401052407
Company information
- Manufacturer
- STRATPHARMA AG;; HiMedica Ltd.
- Manufacturer Country
- United Kingdom;;Switzerland
- Authorized Representative
- EVAPHARM TAIWAN LTD.
Product details
- Intended Use
- Limited to the first level identification range of "Silicone Sheet (I.4025)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4025 Silicone products for scar treatment
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Jun 29, 2011
- Expiry Date
- Jun 29, 2016
- Cancellation Date
- May 21, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Sudamix gel (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 497735abc6893913257490561df56d6a and manufactured by STRATPHARMA AG;; HiMedica Ltd.. The authorized representative in Taiwan is EVAPHARM TAIWAN 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