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"Guomu" compressor type atomizer - Taiwan Registration 46a9e8bfc0b75305bb5786512fc8ca80

Access comprehensive regulatory information for "Guomu" compressor type atomizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 46a9e8bfc0b75305bb5786512fc8ca80 and manufactured by MERITS HEALTH PRODUCTS CO., LTD.. The authorized representative in Taiwan is MERITS HEALTH PRODUCTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Guomu Industry Co., Ltd. General Factory, 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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46a9e8bfc0b75305bb5786512fc8ca80
Registration Details
Taiwan FDA Registration: 46a9e8bfc0b75305bb5786512fc8ca80
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Device Details

"Guomu" compressor type atomizer
TW: "ๅœ‹็ฆ"ๅฃ“็ธฎๆฉŸๅž‹้œงๅŒ–ๅ™จ
Risk Class 2

Registration Details

46a9e8bfc0b75305bb5786512fc8ca80

DHY00500210700

Company Information

Taiwan, Province of China

Product Details

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

D Anesthesiology

D.5630 Nebulizer

Domestic

Dates and Status

Dec 19, 2006

Dec 19, 2011

Jul 24, 2007

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