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“OMRON” Mesh Nebulizer - Taiwan Registration e1442461b6b73bb5017fde8efc738b89

Access comprehensive regulatory information for “OMRON” Mesh Nebulizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e1442461b6b73bb5017fde8efc738b89 and manufactured by OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY. The authorized representative in Taiwan is OMRON HEALTHCARE TAIWAN 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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e1442461b6b73bb5017fde8efc738b89
Registration Details
Taiwan FDA Registration: e1442461b6b73bb5017fde8efc738b89
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Device Details

“OMRON” Mesh Nebulizer
TW: “歐姆龍”網眼式噴霧器
Risk Class 2
MD

Registration Details

e1442461b6b73bb5017fde8efc738b89

Ministry of Health Medical Device Import No. 032313

DHA05603231302

Company Information

Product Details

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

D Devices for anesthesiology

D5630 Sprayer

Imported from abroad

Dates and Status

Mar 26, 2019

Mar 26, 2024