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"DORNIER" laser with light pipe - Taiwan Registration 1a6e10ff298ef64f28fdb993a2d5b5b0

Access comprehensive regulatory information for "DORNIER" laser with light pipe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1a6e10ff298ef64f28fdb993a2d5b5b0 and manufactured by DORNIER MEDTECH GMBH; Dornier MedTech Laser GmbH. The authorized representative in Taiwan is VICTORY EIGHT ENTERPRISE 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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1a6e10ff298ef64f28fdb993a2d5b5b0
Registration Details
Taiwan FDA Registration: 1a6e10ff298ef64f28fdb993a2d5b5b0
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Device Details

"DORNIER" laser with light pipe
TW: โ€œๅคšๅฐผ็ˆพโ€้›ทๅฐ„็”จๅ…‰ๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

1a6e10ff298ef64f28fdb993a2d5b5b0

DHA00602225209

Company Information

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

Mar 29, 2011

Mar 29, 2021

Jun 15, 2023

Cancellation Information

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