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"Elgen" atomization treatment system - Taiwan Registration 1c6f9acb2a6b0203bad5a12b1bce9fbb

Access comprehensive regulatory information for "Elgen" atomization treatment system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1c6f9acb2a6b0203bad5a12b1bce9fbb and manufactured by Aerogen Ltd., M&M Qualtech Ltd.; Aerogen Ltd.. The authorized representative in Taiwan is TRANSCORE 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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1c6f9acb2a6b0203bad5a12b1bce9fbb
Registration Details
Taiwan FDA Registration: 1c6f9acb2a6b0203bad5a12b1bce9fbb
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Device Details

"Elgen" atomization treatment system
TW: โ€œๆ„›็ˆพ็œŸโ€้œงๅŒ–ๆฒป็™‚็ณป็ตฑ
Risk Class 2

Registration Details

1c6f9acb2a6b0203bad5a12b1bce9fbb

DHA05602861302

Company Information

Product Details

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

D Anesthesiology

D.5630 Nebulizer

import

Dates and Status

Jun 22, 2016

Jun 22, 2026