Taiwan FDA registration 1051f66d257a4dca058366c91b25b1a3
"Picoca" neodymium chromium picosecond laser system
TW: “皮可卡”釹雅鉻皮秒雷射系統
Taiwan·Risk Class 2·KL Inc.·Registered Mar 26, 2024 – Mar 26, 2029ActiveRegistration details
- Analysis ID
- 1051f66d257a4dca058366c91b25b1a3
- Customs Code
- DHA05603712500
Company information
- Manufacturer
- KL Inc.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- DIAMOND BIOTECHNOLOGY 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)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- import
Dates and status
- Registration Date
- Mar 26, 2024
- Expiry Date
- Mar 26, 2029
About this record
Access comprehensive regulatory information for "Picoca" neodymium chromium picosecond 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 1051f66d257a4dca058366c91b25b1a3 and manufactured by KL Inc.. The authorized representative in Taiwan is DIAMOND BIOTECHNOLOGY CO., LTD..
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