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“MAQUET” Ventilator System - Taiwan Registration ce9a3bf994a533a08462cf9c3a99f689

Access comprehensive regulatory information for “MAQUET” Ventilator System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ce9a3bf994a533a08462cf9c3a99f689 and manufactured by MAQUET CRITICAL CARE AB. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MAQUET CRITICAL CARE AB, and 1 recent registrations in the same category. 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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ce9a3bf994a533a08462cf9c3a99f689
Registration Details
Taiwan FDA Registration: ce9a3bf994a533a08462cf9c3a99f689
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Device Details

“MAQUET” Ventilator System
TW: “邁柯唯”呼吸機
Risk Class 2
MD

Registration Details

ce9a3bf994a533a08462cf9c3a99f689

Ministry of Health Medical Device Import No. 028633

DHA05602863305

Company Information

Sweden

Product Details

For details, it is Chinese approved copy of the imitation order

D Devices for anesthesiology

D5895 Continuous breathing apparatus

Imported from abroad

Dates and Status

Jul 14, 2016

Jul 14, 2026

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