Pure Global

“LASEROPTEK” PicoLo Nd:YAG Picosecond Laser System - Taiwan Registration 5961859d32929e50d3fbf5d37e5f7537

Access comprehensive regulatory information for “LASEROPTEK” PicoLo Nd:YAG Picosecond 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 5961859d32929e50d3fbf5d37e5f7537 and manufactured by LASEROPTEK Co., Ltd.. The authorized representative in Taiwan is WOH MEDICAL 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
5961859d32929e50d3fbf5d37e5f7537
Registration Details
Taiwan FDA Registration: 5961859d32929e50d3fbf5d37e5f7537
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“LASEROPTEK” PicoLo Nd:YAG Picosecond Laser System
TW: “雷射歐普克”皮可柔銣雅鉻皮秒雷射系統
Risk Class 2
MD

Registration Details

5961859d32929e50d3fbf5d37e5f7537

Ministry of Health Medical Device Import No. 032689

DHA05603268908

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

Jun 13, 2019

Jun 13, 2024