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"Leishi" double positive pressure respiratory system - Taiwan Registration fe47ca8b4b19901751d639f7062ca44d

Access comprehensive regulatory information for "Leishi" double 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 fe47ca8b4b19901751d639f7062ca44d and manufactured by RESPIRONICS, INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 3 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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fe47ca8b4b19901751d639f7062ca44d
Registration Details
Taiwan FDA Registration: fe47ca8b4b19901751d639f7062ca44d
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Device Details

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

Registration Details

fe47ca8b4b19901751d639f7062ca44d

DHA00602449101

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

Mar 07, 2013

Mar 07, 2028