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"Leishi" positive pressure respiratory system - Taiwan Registration 2f222a923ddf0ae280950950a0021421

Access comprehensive regulatory information for "Leishi" positive pressure respiratory system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2f222a923ddf0ae280950950a0021421 and manufactured by RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including RESPIRONICS INC., RESPIRONICS INC.;; Respironics, Inc., and 5 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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2f222a923ddf0ae280950950a0021421
Registration Details
Taiwan FDA Registration: 2f222a923ddf0ae280950950a0021421
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Device Details

"Leishi" positive pressure respiratory system
TW: โ€œ็ฃŠไป•โ€้™ฝๅฃ“ๅ‘ผๅธ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

2f222a923ddf0ae280950950a0021421

DHA00602424407

Company Information

United States

Product Details

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

D Anesthesiology

D.5905 Non-continuous respirators

import

Dates and Status

Dec 05, 2012

Dec 05, 2022

Apr 12, 2024

Cancellation Information

Logged out

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