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"Leishi" comfort mask - Taiwan Registration 0302a58f36173fae7d91b52b16ee634c

Access comprehensive regulatory information for "Leishi" comfort mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0302a58f36173fae7d91b52b16ee634c 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, 1 companies making similar products including Respironics Inc.;; Respironics Medical Products(Shenzhen)Co., Ltd., 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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0302a58f36173fae7d91b52b16ee634c
Registration Details
Taiwan FDA Registration: 0302a58f36173fae7d91b52b16ee634c
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Device Details

"Leishi" comfort mask
TW: โ€œ็ฃŠไป•โ€่ˆ’้ฉ้ข็ฝฉ
Risk Class 2
Cancelled

Registration Details

0302a58f36173fae7d91b52b16ee634c

DHA04200045301

Company Information

Product Details

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

D Anesthesiology

D.5905 Non-continuous respirators

Input;; Contract manufacturing

Dates and Status

Jul 31, 2012

Jul 31, 2017

Dec 13, 2019

Cancellation Information

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