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“DERMACARE” Intense Pulsed Light System - Taiwan Registration 73a401c1408ad1913248e76663537b77

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 73a401c1408ad1913248e76663537b77 and manufactured by Demacai Co., Ltd. Nanke Branch. The authorized representative in Taiwan is DERMACARE BIOMED INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DERMACARE BIOMED INC., 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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73a401c1408ad1913248e76663537b77
Registration Details
Taiwan FDA Registration: 73a401c1408ad1913248e76663537b77
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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

73a401c1408ad1913248e76663537b77

Ministry of Health Medical Device Manufacturing No. 004232

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

Nov 05, 2013

Nov 05, 2018

May 19, 2022

Cancellation Information

Logged out

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