Pure Global

“Daeshin” NdYAG Laser System - Taiwan Registration 2276de0eb1a5aa3dc37cd8de0c773f7e

Access comprehensive regulatory information for “Daeshin” NdYAG 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 2276de0eb1a5aa3dc37cd8de0c773f7e and manufactured by Daeshin Enterprise Co., Ltd.. The authorized representative in Taiwan is ABIO MEDICAL SYSTEM COPR..

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
2276de0eb1a5aa3dc37cd8de0c773f7e
Registration Details
Taiwan FDA Registration: 2276de0eb1a5aa3dc37cd8de0c773f7e
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Daeshin” NdYAG Laser System
TW: “黛欣”釹雅鉻雷射系統
Risk Class 2
MD

Registration Details

2276de0eb1a5aa3dc37cd8de0c773f7e

Ministry of Health Medical Device Import No. 036272

DHA05603627208

Company Information

Korea, Republic of

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

Imported from abroad

Dates and Status

Jan 11, 2023

Jan 11, 2028