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“Asclepion” Dermablate Er:YAG Laser - Taiwan Registration 2eec97fa576ba12692e3ff7ddc0ab8d9

Access comprehensive regulatory information for “Asclepion” Dermablate Er:YAG Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2eec97fa576ba12692e3ff7ddc0ab8d9 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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2eec97fa576ba12692e3ff7ddc0ab8d9
Registration Details
Taiwan FDA Registration: 2eec97fa576ba12692e3ff7ddc0ab8d9
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Device Details

“Asclepion” Dermablate Er:YAG Laser
TW: “阿斯克比恩”鉺雅鉻皮膚雷射儀
Risk Class 2
MD

Registration Details

2eec97fa576ba12692e3ff7ddc0ab8d9

Ministry of Health Medical Device Import No. 026311

DHA05602631102

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

Jun 16, 2014

Jun 16, 2024