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“Optotek” Medical Therapeutic Laser Diode System - Taiwan Registration e5f8b5408838b7b0d33cb0b2b21f5bdf

Access comprehensive regulatory information for “Optotek” Medical Therapeutic Laser Diode System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e5f8b5408838b7b0d33cb0b2b21f5bdf and manufactured by OPTOTEK D.O.O.. The authorized representative in Taiwan is CLINICO INC..

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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e5f8b5408838b7b0d33cb0b2b21f5bdf
Registration Details
Taiwan FDA Registration: e5f8b5408838b7b0d33cb0b2b21f5bdf
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Device Details

“Optotek” Medical Therapeutic Laser Diode System
TW: “歐普特”二極體雷射治療系統
Risk Class 2
MD
Cancelled

Registration Details

e5f8b5408838b7b0d33cb0b2b21f5bdf

Ministry of Health Medical Device Import No. 029032

DHA05602903200

Company Information

Slovenia

Product Details

M Ophthalmic devices

M4390 Ophthalmic laser unit

Imported from abroad

Dates and Status

Nov 14, 2016

Nov 14, 2021

Dec 03, 2019

Cancellation Information

Logged out

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