Taiwan FDA registration bf4ad4574138c5ade835f03b5657f16f
“LASEROPTEK” Helios IV 785 Q-switched Nd:YAG Laser
TW: “雷射歐普克”第四代海力歐神Q開關式釹雅鉻雷射
Taiwan·Risk Class 2·MD·LASEROPTEK Co., Ltd.·Registered Sep 15, 2022 – Sep 15, 2027ActiveRegistration details
- Analysis ID
- bf4ad4574138c5ade835f03b5657f16f
- License Form
- Ministry of Health Medical Device Import No. 035849
- Customs Code
- DHA05603584906
Company information
- Manufacturer
- LASEROPTEK Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- WOH 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
- Sep 15, 2022
- Expiry Date
- Sep 15, 2027
About this record
Access comprehensive regulatory information for “LASEROPTEK” Helios IV 785 Q-switched Nd:YAG Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bf4ad4574138c5ade835f03b5657f16f and manufactured by LASEROPTEK Co., Ltd.. The authorized representative in Taiwan is WOH MEDICAL CO., LTD..
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