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“ERBE” FiAPC probe - Taiwan Registration 25a8d8a557ed5f174eed78686c5f4cc4

Access comprehensive regulatory information for “ERBE” FiAPC probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 25a8d8a557ed5f174eed78686c5f4cc4 and manufactured by ERBE ELEKTROMEDIZIN GMBH. The authorized representative in Taiwan is ERA BIOTEQ ENTERPRISE 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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25a8d8a557ed5f174eed78686c5f4cc4
Registration Details
Taiwan FDA Registration: 25a8d8a557ed5f174eed78686c5f4cc4
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Device Details

“ERBE” FiAPC probe
TW: “艾柏”氬氣離子凝結用探頭
Risk Class 2
MD

Registration Details

25a8d8a557ed5f174eed78686c5f4cc4

Department of Health Medical Device Import No. 024212

DHA00602421207

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

I General and plastic surgical devices

I4400 Electric knife for cutting and hemostasis and its accessories

Imported from abroad

Dates and Status

Dec 02, 2012

Dec 02, 2027