Taiwan FDA registration 07c812a890a785b9bab2b27e0c593ce2

“Smedtrum” Intense Pulsed Light System

TW: “世渼創”脈衝光儀

Taiwan·Risk Class 2·MD·Smedtrum Medical Technology Co., Ltd.·Registered Aug 23, 2023 – Aug 23, 2028Active

Registration details

Analysis ID: 07c812a890a785b9bab2b27e0c593ce2
License Form: Ministry of Health Medical Device Manufacturing No. 007891

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 23, 2023
Expiry Date: Aug 23, 2028

About this record

Access comprehensive regulatory information for “Smedtrum” Intense Pulsed Light System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 07c812a890a785b9bab2b27e0c593ce2 and manufactured by Smedtrum Medical Technology Co., Ltd.. The authorized representative in Taiwan is Smedtrum Medical Technology Co., Ltd..

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