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Teleflex endotracheal probe (unsterilized) - Taiwan Registration be35d53d5cfb26226e93500cd1297ee2

Access comprehensive regulatory information for Teleflex endotracheal probe (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number be35d53d5cfb26226e93500cd1297ee2 and manufactured by TELEFLEX MEDICAL SDN. BHD.. The authorized representative in Taiwan is Hehua 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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be35d53d5cfb26226e93500cd1297ee2
Registration Details
Taiwan FDA Registration: be35d53d5cfb26226e93500cd1297ee2
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Device Details

Teleflex endotracheal probe (unsterilized)
TW: "ๆณฐๅˆฉ็ฆ" ๆฐฃ็ฎกๅ…ง็ฎกๆŽข้‡ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

be35d53d5cfb26226e93500cd1297ee2

DHA04401208300

Company Information

Malaysia

Product Details

Limited to the first level recognition range of endotracheal tube probe (D.5790) of the management method for medical equipment.

D Anesthesiology

D.5790 ๆฐฃ็ฎกๅ…ง็ฎกๆŽข้‡

import

Dates and Status

Aug 20, 2012

Aug 20, 2017

Sep 10, 2018

Cancellation Information

Logged out

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