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“YERIM” Q-Switched Nd:YAG Laser System - Taiwan Registration ba298c729e7d0a4f24c5b0825911722d

Access comprehensive regulatory information for “YERIM” Q-Switched Nd:YAG 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 ba298c729e7d0a4f24c5b0825911722d and manufactured by Yerim Engineering Co., Ltd.. The authorized representative in Taiwan is K2 INTERNATIONAL MEDICAL INC..

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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ba298c729e7d0a4f24c5b0825911722d
Registration Details
Taiwan FDA Registration: ba298c729e7d0a4f24c5b0825911722d
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Device Details

“YERIM” Q-Switched Nd:YAG Laser System
TW: “藝林”Q開關釹雅各雷射系統
Risk Class 2
MD

Registration Details

ba298c729e7d0a4f24c5b0825911722d

Ministry of Health Medical Device Import No. 030240

DHA05603024004

Company Information

Korea, Republic of

Product Details

For details, it is Chinese approved copy of the imitation order

I General and plastic surgical devices

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

Sep 20, 2017

Sep 20, 2022