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"Accriva" Tenderfoot Incision Instruments (Non-Sterile) - Taiwan Registration a11640eac9ecee598b7f1e0377332cc8

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 a11640eac9ecee598b7f1e0377332cc8 and manufactured by Accriva Diagnostics Inc., dba ITC, dba Accumetrics. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ACCRIVA DIAGNOSTICS, 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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a11640eac9ecee598b7f1e0377332cc8
Registration Details
Taiwan FDA Registration: a11640eac9ecee598b7f1e0377332cc8
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Device Details

"Accriva" Tenderfoot Incision Instruments (Non-Sterile)
TW: "่‰พๅฅŽ็™ผ" ่…ณ่ทŸๆŽก่ก€ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a11640eac9ecee598b7f1e0377332cc8

Ministry of Health Medical Device Import No. 017061

DHA09401706108

Company Information

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 06, 2016

Oct 06, 2021

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