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"Artini" transilluminator (unsterilized) - Taiwan Registration f36cc4f2db2d5eb02e3d04b212dc0781

Access comprehensive regulatory information for "Artini" transilluminator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f36cc4f2db2d5eb02e3d04b212dc0781 and manufactured by ARTINIS MEDICAL SYSTEMS B.V.. The authorized representative in Taiwan is MICROSTAR INSTRUMENTS 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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f36cc4f2db2d5eb02e3d04b212dc0781
Registration Details
Taiwan FDA Registration: f36cc4f2db2d5eb02e3d04b212dc0781
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Device Details

"Artini" transilluminator (unsterilized)
TW: "ไบžๅ คๅฐผ"้€็…งๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

f36cc4f2db2d5eb02e3d04b212dc0781

DHA04401145700

Company Information

Netherlands

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Translucent Apparatus (M.1945)".

M Ophthalmology

M.1945 Transilluminator

import

Dates and Status

Mar 09, 2012

Mar 09, 2017

Apr 10, 2017

Cancellation Information

Logged out

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