Taiwan FDA registration 4ec164d86bdc2b46ff2328c5dae9d605
"Chimead" is attached to a syringe
TW: “奇美德”清麗朗附注射器
Taiwan·Risk Class 3·Q-MED AB·Registered Oct 14, 2011 – Oct 14, 2016CancelledRegistration details
- Analysis ID
- 4ec164d86bdc2b46ff2328c5dae9d605
- Customs Code
- DHA00602290107
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
- Product Type (Level 2)
- I.0002 Collagen implants
- Import Information
- import
Dates and status
- Registration Date
- Oct 14, 2011
- Expiry Date
- Oct 14, 2016
- Cancellation Date
- May 14, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期;;自請註銷
About this record
Access comprehensive regulatory information for "Chimead" is 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 4ec164d86bdc2b46ff2328c5dae9d605 and manufactured by Q-MED AB. The authorized representative in Taiwan is GALDERMA HONG KONG LIMITED, TAIWAN BRANCH.
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