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"Miesio" non-powered neurosurgical instruments (unsterilized) - Taiwan Registration 1036fd4ba1de4532cb8d0d6944a29741

Access comprehensive regulatory information for "Miesio" non-powered neurosurgical instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1036fd4ba1de4532cb8d0d6944a29741 and manufactured by MIZUHO AMERICA, INC.. The authorized representative in Taiwan is BARRY TEC 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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1036fd4ba1de4532cb8d0d6944a29741
Registration Details
Taiwan FDA Registration: 1036fd4ba1de4532cb8d0d6944a29741
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Device Details

"Miesio" non-powered neurosurgical instruments (unsterilized)
TW: โ€œๅฏ†ๆ–ฏๅฅงโ€ ้žๅ‹•ๅŠ›ๅผ็ฅž็ถ“ๅค–็ง‘็”จๅ™จๆขฐ๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1
Cancelled

Registration Details

1036fd4ba1de4532cb8d0d6944a29741

DHA04400831700

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Neurosurgical Devices (K.4535)".

K Neuroscience

K.4535 ้žๅ‹•ๅŠ›ๅผ็ฅž็ถ“ๅค–็ง‘็”จๅ™จๆขฐ

import

Dates and Status

Nov 25, 2009

Nov 25, 2014

Aug 09, 2018

Cancellation Information

Logged out

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