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“OMRON” UltraSonic Nebulizer - Taiwan Registration 1ac41a48c959123fd57d0c56eb4b10c2

Access comprehensive regulatory information for “OMRON” UltraSonic Nebulizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1ac41a48c959123fd57d0c56eb4b10c2 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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1ac41a48c959123fd57d0c56eb4b10c2
Registration Details
Taiwan FDA Registration: 1ac41a48c959123fd57d0c56eb4b10c2
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Device Details

“OMRON” UltraSonic Nebulizer
TW: “歐姆龍” 超音波噴霧治療器
Risk Class 2
MD

Registration Details

1ac41a48c959123fd57d0c56eb4b10c2

Ministry of Health Medical Device Import No. 029670

DHA05602967003

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

Apr 21, 2017

Apr 21, 2027