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“Simex” Subglottic aspiration system - Taiwan Registration 1a7b889b27bf846387b8f066f32d9cfa

Access comprehensive regulatory information for “Simex” Subglottic aspiration system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1a7b889b27bf846387b8f066f32d9cfa and manufactured by Simex Medizintechnik GmbH. The authorized representative in Taiwan is BIOSYSTEMS 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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1a7b889b27bf846387b8f066f32d9cfa
Registration Details
Taiwan FDA Registration: 1a7b889b27bf846387b8f066f32d9cfa
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Device Details

“Simex” Subglottic aspiration system
TW: “賽麥斯”聲門下抽吸系統
Risk Class 2
MD

Registration Details

1a7b889b27bf846387b8f066f32d9cfa

Ministry of Health Medical Device Import No. 034593

DHA05603459305

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

I General and plastic surgical devices

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Imported from abroad

Dates and Status

Jun 09, 2021

Jun 09, 2026