Taiwan FDA registration def8be84b6ceb52f4beb33e4ac1e2d1e
“BlueCore” Picosecond Nd:Yag Laser System
TW: “藍芯”皮秒雷射系統
Taiwan·Risk Class 2·MD·Bluecore Company·Registered Oct 06, 2022 – Oct 06, 2027ActiveRegistration details
- Analysis ID
- def8be84b6ceb52f4beb33e4ac1e2d1e
- License Form
- Ministry of Health Medical Device Import No. 035922
- Customs Code
- DHA05603592203
Company information
- Manufacturer
- Bluecore Company
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- PRIMESTAR MEDICAL 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
- Oct 06, 2022
- Expiry Date
- Oct 06, 2027
About this record
Access comprehensive regulatory information for “BlueCore” Picosecond 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 def8be84b6ceb52f4beb33e4ac1e2d1e and manufactured by Bluecore Company. The authorized representative in Taiwan is PRIMESTAR MEDICAL CO., LTD..
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