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“ADEOR” Manual surgical instrument for general use (Non-Sterile) - Taiwan Registration a0567f5889c73474e561e2a3705fc8bb

Access comprehensive regulatory information for “ADEOR” 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 a0567f5889c73474e561e2a3705fc8bb and manufactured by ADEOR MEDICAL AG. The authorized representative in Taiwan is Shiang Tai Medical Instructment 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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a0567f5889c73474e561e2a3705fc8bb
Registration Details
Taiwan FDA Registration: a0567f5889c73474e561e2a3705fc8bb
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Device Details

“ADEOR” Manual surgical instrument for general use (Non-Sterile)
TW: “艾德爾”一般手術用手動式器械 (未滅菌)
Risk Class 1
MD

Registration Details

a0567f5889c73474e561e2a3705fc8bb

Ministry of Health Medical Device Import No. 022237

DHA09402223700

Company Information

Germany

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Jan 08, 2021

Jan 08, 2026