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“HONG SHIANG” NEBULIZER - Taiwan Registration aaae603f5d325fd89bfb2c23099f6b21

Access comprehensive regulatory information for “HONG SHIANG” NEBULIZER in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aaae603f5d325fd89bfb2c23099f6b21 and manufactured by HONG SHIANG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HONG SHIANG TECHNOLOGY 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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aaae603f5d325fd89bfb2c23099f6b21
Registration Details
Taiwan FDA Registration: aaae603f5d325fd89bfb2c23099f6b21
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Device Details

“HONG SHIANG” NEBULIZER
TW: “鴻祥” 噴霧治療器
Risk Class 2
MD

Registration Details

aaae603f5d325fd89bfb2c23099f6b21

Ministry of Health Medical Device Manufacturing No. 007314

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

D Devices for anesthesiology

D5630 Sprayer

Produced in Taiwan, China

Dates and Status

Oct 18, 2021

Oct 18, 2026