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“Quanta” I-Dust Laser System - Taiwan Registration f631c2d94ef4f798ac57353d2a45728c

Access comprehensive regulatory information for “Quanta” I-Dust 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 f631c2d94ef4f798ac57353d2a45728c and manufactured by Quanta System S.p.A. The authorized representative in Taiwan is LITHO MED TRADING 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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f631c2d94ef4f798ac57353d2a45728c
Registration Details
Taiwan FDA Registration: f631c2d94ef4f798ac57353d2a45728c
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Device Details

“Quanta” I-Dust Laser System
TW: “寬達”艾達斯雷射系統
Risk Class 2
MD

Registration Details

f631c2d94ef4f798ac57353d2a45728c

Ministry of Health Medical Device Import No. 031554

DHA05603155406

Company Information

Italy

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

Aug 10, 2018

Aug 10, 2028