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"Leishi" positive pressure respiratory system - Taiwan Registration 6f63f325127c8ce62ac2886a3cebe7f6

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 6f63f325127c8ce62ac2886a3cebe7f6 and manufactured by RESPIRONICS INC.;; 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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6f63f325127c8ce62ac2886a3cebe7f6
Registration Details
Taiwan FDA Registration: 6f63f325127c8ce62ac2886a3cebe7f6
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Device Details

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

Registration Details

6f63f325127c8ce62ac2886a3cebe7f6

DHA05603256302

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

Apr 11, 2019

Apr 11, 2029

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