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"Accriva" Tenderfoot Incision Instruments (Non-Sterile) - Taiwan Registration 3d0c9a340944d920d40d06e7cd03fb21

Access comprehensive regulatory information for "Accriva" Tenderfoot 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 3d0c9a340944d920d40d06e7cd03fb21 and manufactured by ACCRIVA DIAGNOSTICS. The authorized representative in Taiwan is BioChain Co., Ltd..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Accriva Diagnostics Inc., dba ITC, dba Accumetrics, and 1 recent registrations in the same category. 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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3d0c9a340944d920d40d06e7cd03fb21
Registration Details
Taiwan FDA Registration: 3d0c9a340944d920d40d06e7cd03fb21
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Device Details

"Accriva" Tenderfoot Incision Instruments (Non-Sterile)
TW: "ๆ„›่‘ต็™ผ" ่…ณ่ทŸๆŽก่ก€ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

3d0c9a340944d920d40d06e7cd03fb21

Ministry of Health Medical Device Import No. 017127

DHA09401712702

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

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