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"Active" endotracheal tube fixation belt (unsterilized) - Taiwan Registration 365ac7895d50e2161d6c97ae8c9f6147

Access comprehensive regulatory information for "Active" endotracheal tube fixation belt (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 365ac7895d50e2161d6c97ae8c9f6147 and manufactured by FERNO-WASHINGTON, INC.. The authorized representative in Taiwan is TARGETLINE INCORPORATED.

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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365ac7895d50e2161d6c97ae8c9f6147
Registration Details
Taiwan FDA Registration: 365ac7895d50e2161d6c97ae8c9f6147
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Device Details

"Active" endotracheal tube fixation belt (unsterilized)
TW: "ๆดป็ตก"ๆฐฃ็ฎกๅ…ง็ฎกๅ›บๅฎšๅธถ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

365ac7895d50e2161d6c97ae8c9f6147

DHA04400380103

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Tracheal Pipeline Fixation Device (D.5770)".

D Anesthesiology

D.5770 ๆฐฃ็ฎก็ฎก่ทฏๅ›บๅฎš่ฃ็ฝฎ

import

Dates and Status

Apr 13, 2006

Apr 13, 2011

Oct 29, 2012

Cancellation Information

Logged out

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