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EPS EASYMAX Lanzo Lancing Device (Non-Sterile) - Taiwan Registration 576f0c00f8b6c9a22d116b6ea1af9bb0

Access comprehensive regulatory information for EPS EASYMAX Lanzo Lancing Device (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 576f0c00f8b6c9a22d116b6ea1af9bb0 and manufactured by GMMC (Global Medical Market Corporation). The authorized representative in Taiwan is EPS BIO TECHNOLOGY CORP..

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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576f0c00f8b6c9a22d116b6ea1af9bb0
Registration Details
Taiwan FDA Registration: 576f0c00f8b6c9a22d116b6ea1af9bb0
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Device Details

EPS EASYMAX Lanzo Lancing Device (Non-Sterile)
TW: ็ฆๆฐธๅฎœ็‘ชๆฐ้›ท็ขฉๆŽก่ก€็ญ†(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

576f0c00f8b6c9a22d116b6ea1af9bb0

Ministry of Health Medical Device Import No. 021094

DHA09402109402

Company Information

Korea, Republic of

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 12, 2019

Dec 12, 2024