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"Leishi" Cerobi mask - Taiwan Registration f5177246461808cb6e6120032dbd21e9

Access comprehensive regulatory information for "Leishi" Cerobi mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f5177246461808cb6e6120032dbd21e9 and manufactured by RESPIRONICS INC.;; RESPIRONICS MEDICAL PRODUCTS (SZ) CO., LTD.. 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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f5177246461808cb6e6120032dbd21e9
Registration Details
Taiwan FDA Registration: f5177246461808cb6e6120032dbd21e9
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Device Details

"Leishi" Cerobi mask
TW: โ€œ็ฃŠไป•โ€ ่ณฝ่‹ฅๆฏ”้ข็ฝฉ
Risk Class 2

Registration Details

f5177246461808cb6e6120032dbd21e9

DHA09200144003

Company Information

Product Details

Details are as detailed as approved Chinese instructions

D Anesthesiology

D.5905 Non-continuous respirators

Chinese goods;; input

Dates and Status

Apr 20, 2023

Apr 20, 2028