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“Asclepion” QuadroStarPRO Laser - Taiwan Registration dd42284d1e37ae38cf1eec814fadce4b

Access comprehensive regulatory information for “Asclepion” QuadroStarPRO Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dd42284d1e37ae38cf1eec814fadce4b and manufactured by Asclepion Laser Technologies GmbH. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

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: dd42284d1e37ae38cf1eec814fadce4b
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Device Details

“Asclepion” QuadroStarPRO Laser
TW: “阿斯克比恩”庫卓普羅雷射儀
Risk Class 2
MD

Registration Details

dd42284d1e37ae38cf1eec814fadce4b

Ministry of Health Medical Device Import No. 026775

DHA05602677502

Company Information

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

Nov 06, 2014

Nov 06, 2024