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"DORNIER" Medilor diode laser - Taiwan Registration f481ca02485ca60a2079164af6cc9c95

Access comprehensive regulatory information for "DORNIER" Medilor diode laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f481ca02485ca60a2079164af6cc9c95 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, 1 companies making similar products including DORNIER MEDTECH GMBH; Dornier MedTech Laser GmbH, and 3 recent registrations in the same category. 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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f481ca02485ca60a2079164af6cc9c95
Registration Details
Taiwan FDA Registration: f481ca02485ca60a2079164af6cc9c95
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Device Details

"DORNIER" Medilor diode laser
TW: โ€œๅคšๅฐผ็ˆพโ€็พŽๅธๆจ‚ไบŒๆฅต้ซ”้›ทๅฐ„
Risk Class 2
Cancelled

Registration Details

f481ca02485ca60a2079164af6cc9c95

DHA00602403702

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

Sep 21, 2012

Sep 21, 2017

Dec 13, 2019

Cancellation Information

Logged out

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