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"Aerox" respirator - Taiwan Registration 1c4bcd9e6bf50922534cf16ec906cd84

Access comprehensive regulatory information for "Aerox" respirator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1c4bcd9e6bf50922534cf16ec906cd84 and manufactured by AIROX. The authorized representative in Taiwan is Taiwan Tyco Pharmaceutical Co., Ltd.

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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1c4bcd9e6bf50922534cf16ec906cd84
Registration Details
Taiwan FDA Registration: 1c4bcd9e6bf50922534cf16ec906cd84
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Device Details

"Aerox" respirator
TW: โ€œ่‰พ็พ…ๅ…‹ๆ–ฏโ€ๅ‘ผๅธๅ™จ
Risk Class 2
Cancelled

Registration Details

1c4bcd9e6bf50922534cf16ec906cd84

DHA00601950900

Company Information

France

Product Details

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

D Anesthesiology

D.5905 Non-continuous respirators

import

Dates and Status

Dec 18, 2008

Dec 18, 2013

Apr 23, 2015

Cancellation Information

Logged out

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