Subcutaneous Lidocain-filled gel
Vietnam·Risk Class TTBYT Loại D·Restylane Kysse·Q-Med AB·Registered Apr 10, 2024- Analysis ID
- 2400465ĐKLH/BYT-HTTB
- Submission ID
- 17001167/ĐKLH-BYT-TB-CT
- Product Type
- Restylane Kysse
- Manufacturer
- Q-Med AB
- Manufacturer Country
- SWEDEN
- Product Owner
- Q-Med AB
- Authorized Representative
- CÔNG TY TNHH DKSH VIỆT NAM
- Intended Use
- This product is used to restore or increase the volume of the lips. It should be injected into the submucosal layer of the lip. Lidocaine is added to the formula to reduce pain during the injection process.
- Registration Date
- Apr 10, 2024
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Access comprehensive regulatory information for Subcutaneous Lidocain-filled gel in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại D medical device is registered under number 2400465ĐKLH/BYT-HTTB and manufactured by Q-Med AB. The authorized representative in Vietnam is CÔNG TY TNHH DKSH VIỆT NAM.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Q-Med AB, and 1 recent registrations in the same category. Pure Global AI offers free access to 300,000+ Vietnamese medical device registrations, helping global MedTech companies navigate Vietnam MOH regulations, identify competitors, and discover partnership opportunities efficiently.