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"Leishi" comfort mask - Taiwan Registration dd8f16295922e8c6567aa5edaeec9f1e

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 dd8f16295922e8c6567aa5edaeec9f1e 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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dd8f16295922e8c6567aa5edaeec9f1e
Registration Details
Taiwan FDA Registration: dd8f16295922e8c6567aa5edaeec9f1e
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Device Details

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

Registration Details

dd8f16295922e8c6567aa5edaeec9f1e

DHA04200045403

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

Aug 01, 2012

Aug 01, 2022

Apr 12, 2024

Cancellation Information

Logged out

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