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"Accriva" Tenderlett Incision Instruments (Non-Sterile) - Taiwan Registration 44188efc26b23526f632fff436ff8ae0

Access comprehensive regulatory information for "Accriva" Tenderlett Incision Instruments (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 44188efc26b23526f632fff436ff8ae0 and manufactured by ACCRIVA DIAGNOSTICS. The authorized representative in Taiwan is BioChain 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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44188efc26b23526f632fff436ff8ae0
Registration Details
Taiwan FDA Registration: 44188efc26b23526f632fff436ff8ae0
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Device Details

"Accriva" Tenderlett Incision Instruments (Non-Sterile)
TW: "ๆ„›่‘ต็™ผ" ๆ‰‹ๆŒ‡ๆŽก่ก€ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

44188efc26b23526f632fff436ff8ae0

Ministry of Health Medical Device Import No. 017126

DHA09401712600

Company Information

United States

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

Oct 27, 2016

Oct 27, 2021