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"Lei" oxygen concentrator - Taiwan Registration 81a186cb52ef23dc5f056bd370486647

Access comprehensive regulatory information for "Lei" 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 81a186cb52ef23dc5f056bd370486647 and manufactured by RESPIRONICS INC.. The authorized representative in Taiwan is ASIAMED INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including RESPIRONICS GEORGIA, INC., Flextronics Manufacturing Juรกrez S. de R.L. de C.V.; 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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81a186cb52ef23dc5f056bd370486647
Registration Details
Taiwan FDA Registration: 81a186cb52ef23dc5f056bd370486647
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Device Details

"Lei" oxygen concentrator
TW: โ€œ็ฃŠๅฃซโ€ๆฐงๆฐฃๆฟƒ็ธฎๆฉŸ
Risk Class 2
Cancelled

Registration Details

81a186cb52ef23dc5f056bd370486647

DHA00601888201

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

Jun 02, 2008

Jun 02, 2013

Aug 04, 2015

Cancellation Information

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