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“OMRON” Compressor Nebulizer - Taiwan Registration f265af256e4d0d3213b73e27c08fb483

Access comprehensive regulatory information for “OMRON” Compressor Nebulizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f265af256e4d0d3213b73e27c08fb483 and manufactured by OMRON HEALTHCARE MANUFACTURING VIETNAM CO., LTD.. The authorized representative in Taiwan is OMRON HEALTHCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including OMRON HEALTHCARE MANUFACTURING VIETNAM CO., LTD., 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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f265af256e4d0d3213b73e27c08fb483
Registration Details
Taiwan FDA Registration: f265af256e4d0d3213b73e27c08fb483
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Device Details

“OMRON” Compressor Nebulizer
TW: “歐姆龍”噴霧器
Risk Class 2
MD

Registration Details

f265af256e4d0d3213b73e27c08fb483

Ministry of Health Medical Device Import No. 028151

DHA05602815100

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

Jan 21, 2016

Jan 21, 2026

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