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"Lei" oxygen concentrator - Taiwan Registration b6faa77ebd91092f68e5db6fc294ba30

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 b6faa77ebd91092f68e5db6fc294ba30 and manufactured by RESPIRONICS GEORGIA, 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 Flextronics Manufacturing Juรกrez 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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b6faa77ebd91092f68e5db6fc294ba30
Registration Details
Taiwan FDA Registration: b6faa77ebd91092f68e5db6fc294ba30
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Device Details

"Lei" oxygen concentrator
TW: "็ฃŠๅฃซ"ๆฐงๆฐฃๆฟƒ็ธฎๆฉŸ
Risk Class 2
Cancelled

Registration Details

b6faa77ebd91092f68e5db6fc294ba30

DHA00601707506

Company Information

United States

Product Details

Supplemental oxygen is provided to patients who require low-flow oxygen therapy.

D Anesthesiology

import

Dates and Status

Sep 04, 2006

Sep 04, 2011

Nov 30, 2012

Cancellation Information

Logged out

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