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"Leishi" mask bend - Taiwan Registration 2da992d6c7686206b805009de35c7ad7

Access comprehensive regulatory information for "Leishi" mask bend in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2da992d6c7686206b805009de35c7ad7 and manufactured by RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details. 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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2da992d6c7686206b805009de35c7ad7
Registration Details
Taiwan FDA Registration: 2da992d6c7686206b805009de35c7ad7
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Device Details

"Leishi" mask bend
TW: โ€œ็ฃŠไป•โ€้ข็ฝฉๅฝŽ็ฎก
Risk Class 2

Registration Details

2da992d6c7686206b805009de35c7ad7

DHA00602393901

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

Aug 22, 2012

Aug 22, 2027