Taiwan FDA registration 2e0604d724f21989186390a5c72b5435
"Chimead" Terrilang attached to a syringe
TW: “奇美德”特麗朗附注射器
Taiwan·Risk Class 3·Q-MED AB·Registered Oct 27, 2011 – Oct 27, 2016CancelledRegistration details
- Analysis ID
- 2e0604d724f21989186390a5c72b5435
- Customs Code
- DHA00602297500
Company information
- Manufacturer
- Q-MED AB
- Manufacturer Country
- Sweden
- Authorized Representative
- GALDERMA HONG KONG LIMITED, TAIWAN BRANCH
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
- Oct 27, 2011
- Expiry Date
- Oct 27, 2016
- Cancellation Date
- May 14, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷;;許可證已逾有效期
About this record
Access comprehensive regulatory information for "Chimead" Terrilang attached to a syringe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2e0604d724f21989186390a5c72b5435 and manufactured by Q-MED AB. The authorized representative in Taiwan is GALDERMA HONG KONG LIMITED, TAIWAN BRANCH.
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