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“Maxtec” Air/Oxygen Blender - Taiwan Registration cbe7c8f524bcdbdb66cd9fb1c0a6dcfc

Access comprehensive regulatory information for “Maxtec” Air/Oxygen Blender in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cbe7c8f524bcdbdb66cd9fb1c0a6dcfc and manufactured by MAXTEC, LLC. The authorized representative in Taiwan is FISHER & PAYKEL HEALTHCARE ASIA LIMITED, TAIWAN BRANCH (NEW ZEALAND).

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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cbe7c8f524bcdbdb66cd9fb1c0a6dcfc
Registration Details
Taiwan FDA Registration: cbe7c8f524bcdbdb66cd9fb1c0a6dcfc
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Device Details

“Maxtec” Air/Oxygen Blender
TW: “麥斯特克” 空氣/氧氣混合器
Risk Class 2
MD

Registration Details

cbe7c8f524bcdbdb66cd9fb1c0a6dcfc

Ministry of Health Medical Device Import No. 034879

DHA05603487900

Company Information

Product Details

Details are as detailed as approved Chinese instructions

D Devices for anesthesiology

D5330 Breathing Gas Mixer

Imported from abroad

Dates and Status

Oct 18, 2021

Oct 18, 2026