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“ERBE” LAP Bisect - Taiwan Registration 8f516f1198b96ab9119a05270fb05b6f

Access comprehensive regulatory information for “ERBE” LAP Bisect in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8f516f1198b96ab9119a05270fb05b6f 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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8f516f1198b96ab9119a05270fb05b6f
Registration Details
Taiwan FDA Registration: 8f516f1198b96ab9119a05270fb05b6f
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Device Details

“ERBE” LAP Bisect
TW: “艾柏”腹鏡下百克剪
Risk Class 2
MD

Registration Details

8f516f1198b96ab9119a05270fb05b6f

Department of Health Medical Device Import No. 023608

DHA00602360801

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

May 31, 2012

May 31, 2027