Taiwan FDA registration 54209d89c0dd2652a8b81c7c183395f9
“Lutronic” LaseMD Ultra Thulium Laser System
TW: “儷妮可”雷絲美奧創銩雷射系統
Taiwan·Risk Class 2·MD·Lutronic Corporation·Registered May 20, 2022 – May 20, 2027ActiveRegistration details
- Analysis ID
- 54209d89c0dd2652a8b81c7c183395f9
- License Form
- Ministry of Health Medical Device Import No. 035492
- Customs Code
- DHA05603549204
Company information
- Manufacturer
- Lutronic Corporation
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- VICTORY EIGHT ENTERPRISE CO., LTD.
Product details
- Intended Use
- This product is a 19.2nm thulium laser, suitable for wrinkle improvement, dermabrasion and pigment treatment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 20, 2022
- Expiry Date
- May 20, 2027
About this record
Access comprehensive regulatory information for “Lutronic” LaseMD Ultra Thulium Laser System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 54209d89c0dd2652a8b81c7c183395f9 and manufactured by Lutronic Corporation. The authorized representative in Taiwan is VICTORY EIGHT ENTERPRISE CO., LTD..
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