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"Lucie" endotracheal probe (unsterilized) - Taiwan Registration e43f2f04c4dc005349d1d435ff7d051d

Access comprehensive regulatory information for "Lucie" 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 e43f2f04c4dc005349d1d435ff7d051d and manufactured by RUSCH SDN. BHD.. The authorized representative in Taiwan is TRIPLE ROPES ENTERPRISE 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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e43f2f04c4dc005349d1d435ff7d051d
Registration Details
Taiwan FDA Registration: e43f2f04c4dc005349d1d435ff7d051d
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Device Details

"Lucie" endotracheal probe (unsterilized)
TW: โ€œ่ทฏ่ฅฟโ€ๆฐฃ็ฎกๅ…ง็ฎกๆŽข้‡ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

e43f2f04c4dc005349d1d435ff7d051d

DHA04400480302

Company Information

Malaysia

Product Details

It is limited to the first level of identification of endotracheal probes (D.5790) of the Measures for the Administration of Medical Devices.

D Anesthesiology

D.5790 ๆฐฃ็ฎกๅ…ง็ฎกๆŽข้‡

import

Dates and Status

Jun 28, 2006

Jun 28, 2016

Apr 13, 2018

Cancellation Information

Logged out

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