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"Leishi" Dream Booster Nasal Mask - Taiwan Registration 2de7544a38098903b223793b2a262da7

Access comprehensive regulatory information for "Leishi" Dream Booster Nasal Mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2de7544a38098903b223793b2a262da7 and manufactured by Respironics Inc.;; Respironics Medical Products(Shenzhen)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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2de7544a38098903b223793b2a262da7
Registration Details
Taiwan FDA Registration: 2de7544a38098903b223793b2a262da7
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Device Details

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

Registration Details

2de7544a38098903b223793b2a262da7

DHA09200074902

Company Information

Product Details

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

D Anesthesiology

D.5905 Non-continuous respirators

Input;; Chinese goods

Dates and Status

Mar 16, 2016

Mar 16, 2026