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“RegenLab”Manual surgical instrument for general use (Non-Sterile) - Taiwan Registration 878f3de07a1548b0444465deaf583de3

Access comprehensive regulatory information for “RegenLab”Manual surgical instrument for general use (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 878f3de07a1548b0444465deaf583de3 and manufactured by REGEN LAB SA. The authorized representative in Taiwan is NEOTEC COSMECEUTICAL LIMITED.

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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878f3de07a1548b0444465deaf583de3
Registration Details
Taiwan FDA Registration: 878f3de07a1548b0444465deaf583de3
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Device Details

“RegenLab”Manual surgical instrument for general use (Non-Sterile)
TW: “利奇”一般手術用手動式器械 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

878f3de07a1548b0444465deaf583de3

Ministry of Health Medical Device Import No. 013699

DHA09401369901

Company Information

Switzerland

Product Details

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Dec 19, 2013

Dec 19, 2018

Jul 01, 2015

Cancellation Information

Logged out

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