Pure Global

"Mizuho America" Nonpowered neurosurgical instrument (Non-Sterile) - Taiwan Registration d2756938717a8369cb4177d40182a490

Access comprehensive regulatory information for "Mizuho America" Nonpowered neurosurgical instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d2756938717a8369cb4177d40182a490 and manufactured by MIZUHO AMERICA, INC.. The authorized representative in Taiwan is RUI-HUNG INSTRUMENTS 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
d2756938717a8369cb4177d40182a490
Registration Details
Taiwan FDA Registration: d2756938717a8369cb4177d40182a490
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Mizuho America" Nonpowered neurosurgical instrument (Non-Sterile)
TW: "็พŽๆดฅๅŽ" ้žๅ‹•ๅŠ›ๅผ็ฅž็ถ“ๅค–็ง‘็”จๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d2756938717a8369cb4177d40182a490

Ministry of Health Medical Device Import No. 022160

DHA09402216004

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 Devices for neuroscience

K4535 Non-powered neurosurgical instruments

Imported from abroad

Dates and Status

Dec 07, 2020

Dec 07, 2025