Taiwan FDA registration 7b9c1ecb53b86ab60521f408ae21bd98
Restylane Kysse
TW: 瑞絲朗-漾采(含利多卡因)
Taiwan·Risk Class 3·MD·Q-MED AB·Registered Dec 05, 2017 – Dec 05, 2027ActiveRegistration details
- Analysis ID
- 7b9c1ecb53b86ab60521f408ae21bd98
- License Form
- Ministry of Health Medical Device Import No. 030305
- Customs Code
- DHA05603030506
Company information
- Manufacturer
- Q-MED AB
- Manufacturer Country
- Sweden
- Authorized Representative
- GALDERMA HONG KONG LIMITED, TAIWAN BRANCH
Product details
- Intended Use
- This product can be used to restore or increase lip volume. This product should be injected into the submucosal layer of the lips. Lidocaine is added to the product to reduce pain during therapeutic injections.
- 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
- Dec 05, 2017
- Expiry Date
- Dec 05, 2027
About this record
Access comprehensive regulatory information for Restylane Kysse in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 7b9c1ecb53b86ab60521f408ae21bd98 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.
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