Taiwan FDA registration af706fb20ce8e46d664156718972efea
“Hironic” PICOHI Nd:YAG Laser System
TW: “希洛尼克”皮秒雷射系統
Taiwan·Risk Class 2·MD·Hironic Co., Ltd.·Registered May 17, 2021 – May 17, 2026ExpiredRegistration details
- Analysis ID
- af706fb20ce8e46d664156718972efea
- License Form
- Ministry of Health Medical Device Import No. 034556
- Customs Code
- DHA05603455602
Company information
- Manufacturer
- Hironic Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- COLLAMATRIX CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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 17, 2021
- Expiry Date
- May 17, 2026
About this record
Access comprehensive regulatory information for “Hironic” PICOHI 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 af706fb20ce8e46d664156718972efea and manufactured by Hironic Co., Ltd.. The authorized representative in Taiwan is COLLAMATRIX CO., LTD..
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