Taiwan FDA registration ce9a3bf994a533a08462cf9c3a99f689

“MAQUET” Ventilator System

TW: “邁柯唯”呼吸機
Taiwan flagTaiwan·Risk Class 2·MD·MAQUET CRITICAL CARE AB·Registered Jul 14, 2016 – Jul 14, 2026Expired
Registration details
Analysis ID
ce9a3bf994a533a08462cf9c3a99f689
License Form
Ministry of Health Medical Device Import No. 028633
Customs Code
DHA05602863305
Company information
Manufacturer Country
Sweden
Authorized Representative
GETINGE GROUP TAIWAN CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
D Devices for anesthesiology
Product Type (Level 2)
D5895 Continuous breathing apparatus
Import Information
Imported from abroad
Dates and status
Registration Date
Jul 14, 2016
Expiry Date
Jul 14, 2026
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About this record

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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