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Reid endotracheal tube maintainer (unsterilized) - Taiwan Registration 49af86043b2ffdddb7dd2f71a8174c94

Access comprehensive regulatory information for Reid endotracheal tube maintainer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 49af86043b2ffdddb7dd2f71a8174c94 and manufactured by LAERDAL MEDICAL AS. The authorized representative in Taiwan is Xinyi 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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49af86043b2ffdddb7dd2f71a8174c94
Registration Details
Taiwan FDA Registration: 49af86043b2ffdddb7dd2f71a8174c94
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Device Details

Reid endotracheal tube maintainer (unsterilized)
TW: ้›ทๅพทๆฐฃ็ฎกๅ…ง็ฎก็ถญๆŒๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

49af86043b2ffdddb7dd2f71a8174c94

DHA04400393103

Company Information

Norway

Product Details

Limited to the first level recognition range of breathing tube support (D.5280) of the medical device management method.

D Anesthesiology

D.5280 ๅ‘ผๅธ็ฎก่ทฏๆ”ฏๆ’็‰ฉ

import

Dates and Status

Apr 15, 2006

Apr 15, 2016

Aug 09, 2018

Cancellation Information

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