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"Leishi" oxygen concentrator - Taiwan Registration 35df12a10e3621cd92c90f3c503d6795

Access comprehensive regulatory information for "Leishi" oxygen concentrator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 35df12a10e3621cd92c90f3c503d6795 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 Flextronics Manufacturing Juarez S. de R.L. de C.V.;; RESPIRONICS INC., Respironics, Inc., and 2 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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35df12a10e3621cd92c90f3c503d6795
Registration Details
Taiwan FDA Registration: 35df12a10e3621cd92c90f3c503d6795
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Device Details

"Leishi" oxygen concentrator
TW: โ€œ็ฃŠไป•โ€ๆฐงๆฐฃๆฟƒ็ธฎๆฉŸ
Risk Class 2

Registration Details

35df12a10e3621cd92c90f3c503d6795

DHA05602925902

Company Information

United States

Product Details

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

D Anesthesiology

D.5440 Portable Oxygen Generator

import

Dates and Status

Dec 28, 2016

Dec 28, 2026