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Tenderfoot Heel Incision Device (Sterile) - Taiwan Registration 512739e56d7d79c0b8594367c307f805

Access comprehensive regulatory information for Tenderfoot Heel Incision Device (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 512739e56d7d79c0b8594367c307f805 and manufactured by Accriva Diagnostics Inc.. 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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512739e56d7d79c0b8594367c307f805
Registration Details
Taiwan FDA Registration: 512739e56d7d79c0b8594367c307f805
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Device Details

Tenderfoot Heel Incision Device (Sterile)
TW: ็–ผๅพ—็ฆ่…ณ่ทŸๆŽก่ก€ๅ™จ(ๆป…่Œ)
Risk Class 1
MD

Registration Details

512739e56d7d79c0b8594367c307f805

Ministry of Health Medical Device Import No. 018624

DHA09401862405

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

Dec 19, 2017

Dec 19, 2027