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"Intermetate" laser diode - Taiwan Registration 3fba222befea5cbe9528625f325643be

Access comprehensive regulatory information for "Intermetate" laser diode in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3fba222befea5cbe9528625f325643be and manufactured by INTERMEDIC ARFRAN, S.A.. The authorized representative in Taiwan is EVERMED INTERNATIONAL 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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3fba222befea5cbe9528625f325643be
Registration Details
Taiwan FDA Registration: 3fba222befea5cbe9528625f325643be
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Device Details

"Intermetate" laser diode
TW: โ€œๅ› ็‰น็พŽๅœฐโ€้›ทๅฐ„ไบŒๆฅตๅ„€
Risk Class 2
Cancelled

Registration Details

3fba222befea5cbe9528625f325643be

DHA00602275802

Company Information

Spain

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

Aug 23, 2011

Aug 23, 2021

Sep 08, 2023

Cancellation Information

Logged out

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