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“OMRON” Compressor Nebulizer - Taiwan Registration 5485d014f87d6ee251dcbc23aa30dc1e

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 5485d014f87d6ee251dcbc23aa30dc1e 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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5485d014f87d6ee251dcbc23aa30dc1e
Registration Details
Taiwan FDA Registration: 5485d014f87d6ee251dcbc23aa30dc1e
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Device Details

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

Registration Details

5485d014f87d6ee251dcbc23aa30dc1e

Ministry of Health Medical Device Import No. 026681

DHA05602668106

Company Information

Product Details

D Devices for anesthesiology

D5630 Sprayer

Imported from abroad

Dates and Status

Nov 21, 2014

Nov 21, 2019

Jun 22, 2022

Cancellation Information

Logged out

許可證已逾有效期

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