Taiwan FDA registration 7f4a27e94798a1b058b65af145b59d93
Macrolane VRF 30
TW: 美可朗30
Taiwan·Risk Class 3·MD·Q-MED AB·Registered Jul 30, 2014 – Jul 30, 2019CancelledRegistration details
- Analysis ID
- 7f4a27e94798a1b058b65af145b59d93
- License Form
- Ministry of Health Medical Device Import No. 026462
- Customs Code
- DHA05602646207
Company information
- Manufacturer
- Q-MED AB
- Manufacturer Country
- Sweden
- Authorized Representative
- GALDERMA HONG KONG LIMITED, TAIWAN BRANCH
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I0007 Hyaluronic acid implants
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 30, 2014
- Expiry Date
- Jul 30, 2019
- Cancellation Date
- Jun 11, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Macrolane VRF 30 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 7f4a27e94798a1b058b65af145b59d93 and manufactured by Q-MED AB. The authorized representative in Taiwan is GALDERMA HONG KONG LIMITED, TAIWAN BRANCH.
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