Taiwan FDA registration d91649b866ac4051327614d67dbb2059
“Smedtrum” CO2 Laser System
TW: “世渼創”二氧化碳雷射儀
Taiwan·Risk Class 2·MD·Smedtrum Medical Technology Co., Ltd.·Registered Aug 24, 2022 – Aug 24, 2027ActiveRegistration details
- Analysis ID
- d91649b866ac4051327614d67dbb2059
- License Form
- Ministry of Health Medical Device Manufacturing No. 007525
Company information
- Manufacturer
- Smedtrum Medical Technology Co., Ltd.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Smedtrum Medical Technology 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
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 24, 2022
- Expiry Date
- Aug 24, 2027
About this record
Access comprehensive regulatory information for “Smedtrum” CO2 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 d91649b866ac4051327614d67dbb2059 and manufactured by Smedtrum Medical Technology Co., Ltd.. The authorized representative in Taiwan is Smedtrum Medical Technology Co., Ltd..
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