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“ERBE” BiSect - Taiwan Registration 44556e2fb62c6792a2b2be482f7e000e

Access comprehensive regulatory information for “ERBE” BiSect in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 44556e2fb62c6792a2b2be482f7e000e 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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44556e2fb62c6792a2b2be482f7e000e
Registration Details
Taiwan FDA Registration: 44556e2fb62c6792a2b2be482f7e000e
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Device Details

“ERBE” BiSect
TW: “艾柏”百克剪
Risk Class 2
MD

Registration Details

44556e2fb62c6792a2b2be482f7e000e

Ministry of Health Medical Device Import No. 029937

DHA05602993704

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

Jul 10, 2017

Jul 10, 2022