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"Bosch" tracheal fixture (unsterilized) - Taiwan Registration fdb09382bfe77bbb9c737bb2ccbe12dd

Access comprehensive regulatory information for "Bosch" tracheal fixture (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fdb09382bfe77bbb9c737bb2ccbe12dd and manufactured by POSEY MEXICO. The authorized representative in Taiwan is NSH MEDICAL CORP..

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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fdb09382bfe77bbb9c737bb2ccbe12dd
Registration Details
Taiwan FDA Registration: fdb09382bfe77bbb9c737bb2ccbe12dd
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Device Details

"Bosch" tracheal fixture (unsterilized)
TW: "ๆณขๅธŒ"ๆฐฃ็ฎก็ฎก่ทฏๅ›บๅฎš่ฃ็ฝฎ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

fdb09382bfe77bbb9c737bb2ccbe12dd

DHA04401224602

Company Information

Mexico

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

Oct 12, 2012

Oct 12, 2022

Apr 12, 2024

Cancellation Information

Logged out

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