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“GN” Madsen AccuScreen ABR - Taiwan Registration 0e9a8df06057f29a7d44087b4ff1895d

Access comprehensive regulatory information for “GN” Madsen AccuScreen ABR in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0e9a8df06057f29a7d44087b4ff1895d and manufactured by GN OTOMETRICS A/S. The authorized representative in Taiwan is FORMOSA MEDICAL 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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0e9a8df06057f29a7d44087b4ff1895d
Registration Details
Taiwan FDA Registration: 0e9a8df06057f29a7d44087b4ff1895d
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Device Details

“GN” Madsen AccuScreen ABR
TW: “吉恩”麥迪生新生兒聽力篩檢儀
Risk Class 2
MD
Cancelled

Registration Details

0e9a8df06057f29a7d44087b4ff1895d

Ministry of Health Medical Device Import No. 026608

DHA05602660809

Company Information

Denmark

Product Details

G ENT device

G1050 Audiogram

Imported from abroad

Dates and Status

Sep 16, 2014

Sep 16, 2019

Jun 07, 2022

Cancellation Information

Logged out

許可證已逾有效期