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"Leishi" heated humidifier - Taiwan Registration f433cf6aa915258d5db7f65fa95e4c17

Access comprehensive regulatory information for "Leishi" heated humidifier in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f433cf6aa915258d5db7f65fa95e4c17 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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f433cf6aa915258d5db7f65fa95e4c17
Registration Details
Taiwan FDA Registration: f433cf6aa915258d5db7f65fa95e4c17
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Device Details

"Leishi" heated humidifier
TW: โ€œ็ฃŠไป•โ€ๅŠ ็†ฑๅž‹ๆฝฎๆฟ•ๅ™จ
Risk Class 2

Registration Details

f433cf6aa915258d5db7f65fa95e4c17

DHA00602438601

Company Information

United States

Product Details

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

D Anesthesiology

D.5450 Vapor moisture apparatus for respirators

import

Dates and Status

Jan 08, 2013

Jan 08, 2028