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“Smedtrum” Intense Pulsed Light System - Taiwan Registration 07c812a890a785b9bab2b27e0c593ce2

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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07c812a890a785b9bab2b27e0c593ce2
Registration Details
Taiwan FDA Registration: 07c812a890a785b9bab2b27e0c593ce2
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Device Details

“Smedtrum” Intense Pulsed Light System
TW: “世渼創”脈衝光儀
Risk Class 2
MD

Registration Details

07c812a890a785b9bab2b27e0c593ce2

Ministry of Health Medical Device Manufacturing No. 007891

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4810 Lasers for general surgery, plastic surgery and dermatology

Produced in Taiwan, China

Dates and Status

Aug 23, 2023

Aug 23, 2028