Taiwan FDA registration 82786712387f4c370d4afd85f05f9163
“Ilooda” CuRAS Q-switched Nd:YAG Laser system
TW: “伊路達”庫雷斯Q開關釹雅各雷射
Taiwan·Risk Class 2·MD·ILOODA CO., LTD.·Registered Sep 16, 2022 – Sep 16, 2027ActiveRegistration details
- Analysis ID
- 82786712387f4c370d4afd85f05f9163
- License Form
- Ministry of Health Medical Device Import No. 035903
- Customs Code
- DHA05603590302
Company information
- Manufacturer
- ILOODA CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- COLLAMATRIX CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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
- Sep 16, 2022
- Expiry Date
- Sep 16, 2027
About this record
Access comprehensive regulatory information for “Ilooda” CuRAS Q-switched Nd:YAG 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 82786712387f4c370d4afd85f05f9163 and manufactured by ILOODA CO., LTD.. The authorized representative in Taiwan is COLLAMATRIX CO., LTD..
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