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"Editi" heel lancing device (unsterilized) - Taiwan Registration b0615faad16264268a4459338a0a3e73

Access comprehensive regulatory information for "Editi" heel lancing device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b0615faad16264268a4459338a0a3e73 and manufactured by INTERNATIONAL TECHNIDYNE CORP.. 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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b0615faad16264268a4459338a0a3e73
Registration Details
Taiwan FDA Registration: b0615faad16264268a4459338a0a3e73
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Device Details

"Editi" heel lancing device (unsterilized)
TW: โ€œ่‰พๅธ่ฅฟโ€่…ณ่ทŸๆŽก่ก€ๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

b0615faad16264268a4459338a0a3e73

DHA04401131901

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, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

import

Dates and Status

Jan 20, 2012

Jan 20, 2017

Dec 13, 2019

Cancellation Information

Logged out

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