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“Ace” Manual surgical instrument for general use (Non-sterile) - Taiwan Registration 176f65b23302f8c847ea2f38eb758390

Access comprehensive regulatory information for “Ace” Manual surgical instrument for general use (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 176f65b23302f8c847ea2f38eb758390 and manufactured by ACE KOREA MEDICAL CO., LTD.. The authorized representative in Taiwan is LA MED INTERNATIONAL 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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176f65b23302f8c847ea2f38eb758390
Registration Details
Taiwan FDA Registration: 176f65b23302f8c847ea2f38eb758390
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Device Details

“Ace” Manual surgical instrument for general use (Non-sterile)
TW: “艾斯”一般手術用手動式器械 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

176f65b23302f8c847ea2f38eb758390

Ministry of Health Medical Device Import No. 014124

DHA09401412404

Company Information

Korea, Republic of

Product Details

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

May 12, 2014

May 12, 2019

Aug 20, 2015

Cancellation Information

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