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“DERMACARE” Intense Pulsed Light System - Taiwan Registration 83e4b1d71d8dbdeace0e82076ff05db8

Access comprehensive regulatory information for “DERMACARE” 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 83e4b1d71d8dbdeace0e82076ff05db8 and manufactured by DERMACARE BIOMED INC.. The authorized representative in Taiwan is DERMACARE BIOMED INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Demacai Co., Ltd. Nanke Branch, and 1 recent registrations in the same category. 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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83e4b1d71d8dbdeace0e82076ff05db8
Registration Details
Taiwan FDA Registration: 83e4b1d71d8dbdeace0e82076ff05db8
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Device Details

“DERMACARE” Intense Pulsed Light System
TW: “德瑪凱”脈衝光系統
Risk Class 2
MD
Cancelled

Registration Details

83e4b1d71d8dbdeace0e82076ff05db8

Ministry of Health Medical Device Manufacturing No. 006311

Company Information

Taiwan, Province of China

Product Details

I General and plastic surgical devices

I4810 Lasers for general surgery, plastic surgery and dermatology

Produced in Taiwan, China

Dates and Status

Jan 08, 2019

Jan 08, 2024

Jan 04, 2023

Cancellation Information

Logged out

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