Taiwan FDA registration e0a31dec4dc32cc1e817e1192b78f3c8
"Laser Opp" Helios Q switched rubidium chromium laser
TW: “雷射歐普克”海力歐斯Q開關式銣雅鉻雷射
Taiwan·Risk Class 2·LASEROPTEK Co., Ltd.·Registered Aug 05, 2016 – Aug 05, 2026ActiveRegistration details
- Analysis ID
- e0a31dec4dc32cc1e817e1192b78f3c8
- Customs Code
- DHA05602871701
Company information
- Manufacturer
- LASEROPTEK Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- WOH MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- 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
- Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.
Dates and status
- Registration Date
- Aug 05, 2016
- Expiry Date
- Aug 05, 2026
About this record
Access comprehensive regulatory information for "Laser Opp" Helios Q switched rubidium chromium laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e0a31dec4dc32cc1e817e1192b78f3c8 and manufactured by LASEROPTEK Co., Ltd.. The authorized representative in Taiwan is WOH MEDICAL CO., LTD..
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