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"Retra" Miyan Q-switched neodymium Jacob laser system - Taiwan Registration 56ae83ef8fc44309b28f8f5a8ba1be1e

Access comprehensive regulatory information for "Retra" Miyan Q-switched neodymium Jacob 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 56ae83ef8fc44309b28f8f5a8ba1be1e and manufactured by LTRA GLOBAL 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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56ae83ef8fc44309b28f8f5a8ba1be1e
Registration Details
Taiwan FDA Registration: 56ae83ef8fc44309b28f8f5a8ba1be1e
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Device Details

"Retra" Miyan Q-switched neodymium Jacob laser system
TW: โ€œ้›ท็‰นๆ‹‰โ€ๅช„ๅฆQ้–‹้—œ้‡น้›…ๅ„้›ทๅฐ„็ณป็ตฑ
Risk Class 2

Registration Details

56ae83ef8fc44309b28f8f5a8ba1be1e

DHA05603399201

Company Information

Korea, Republic of

Product Details

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

I General, Plastic Surgery and Dermatology

I.4810 Lasers for general surgical, orthopaedic and dermatological use

import

Dates and Status

Oct 05, 2020

Oct 05, 2025