Taiwan FDA registration c4d5266c19512010365269619d259e74
Shengli Acne Patch (Sterilized/Unsterilized)
TW: 生麗 痘痘貼 (滅菌/未滅菌)
Taiwan·Risk Class 1·DECORTEC CO., LTD.·Registered Jul 11, 2016 – Jul 11, 2021CancelledRegistration details
- Analysis ID
- c4d5266c19512010365269619d259e74
Company information
- Manufacturer
- DECORTEC CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DECORTEC CO., LTD.
Product details
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Hydrophilic Wound Covering Materials (I.4018)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4018 親水性創傷覆蓋材
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Jul 11, 2016
- Expiry Date
- Jul 11, 2021
- Cancellation Date
- Jun 15, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Shengli Acne Patch (Sterilized/Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c4d5266c19512010365269619d259e74 and manufactured by DECORTEC CO., LTD.. The authorized representative in Taiwan is DECORTEC 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