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“LASEROPTEK” PicoLO PREMIUM Nd:YAG Picosecond Laser System - Taiwan Registration bb13de7fa86f206e89c8d759c5f53743

Access comprehensive regulatory information for “LASEROPTEK” PicoLO PREMIUM 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 bb13de7fa86f206e89c8d759c5f53743 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.

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Registration Details
Taiwan FDA Registration: bb13de7fa86f206e89c8d759c5f53743
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Device Details

“LASEROPTEK” PicoLO PREMIUM 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

bb13de7fa86f206e89c8d759c5f53743

Ministry of Health Medical Device Import No. 035558

DHA05603555808

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

Jun 02, 2022

Jun 02, 2027