Taiwan FDA registration 46c065c69fc144bad601844a76d0db6a
“LASEROPTEK” Helios II Q-switched Nd:YAG Laser
TW: “雷射歐普克”海力歐斯Q開關式釹雅鉻雷射
Taiwan·Risk Class 2·MD·LASEROPTEK Co., Ltd.·Registered May 08, 2020 – May 08, 2025ExpiredRegistration details
- Analysis ID
- 46c065c69fc144bad601844a76d0db6a
- License Form
- Ministry of Health Medical Device Import No. 033628
- Customs Code
- DHA05603362806
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 and plastic surgical devices
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 08, 2020
- Expiry Date
- May 08, 2025
About this record
Access comprehensive regulatory information for “LASEROPTEK” Helios II 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 46c065c69fc144bad601844a76d0db6a and manufactured by LASEROPTEK Co., Ltd.. The authorized representative in Taiwan is WOH MEDICAL CO., LTD..
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