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"Leishi" Dream Nose Mask - Taiwan Registration 37aa58ed38c7b6ee53b6d8eff133fa01

Access comprehensive regulatory information for "Leishi" Dream Nose Mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 37aa58ed38c7b6ee53b6d8eff133fa01 and manufactured by Philips de Costa Rica S.R.L.;; RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

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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37aa58ed38c7b6ee53b6d8eff133fa01
Registration Details
Taiwan FDA Registration: 37aa58ed38c7b6ee53b6d8eff133fa01
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Device Details

"Leishi" Dream Nose Mask
TW: โ€œ็ฃŠไป•โ€ ๅŠฉๅคข้ผป้ข็ฝฉ
Risk Class 2

Registration Details

37aa58ed38c7b6ee53b6d8eff133fa01

DHA05603658901

Company Information

Costa Rica;;United States

Product Details

Details are as detailed as approved Chinese instructions

D Anesthesiology

D.5905 Non-continuous respirators

Input;; Contract manufacturing

Dates and Status

Aug 30, 2023

Aug 30, 2028