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“ERBE” Bipolar Forceps - Taiwan Registration 8d9fbef5cce71165712d4bbae14a1d35

Access comprehensive regulatory information for “ERBE” Bipolar Forceps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8d9fbef5cce71165712d4bbae14a1d35 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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8d9fbef5cce71165712d4bbae14a1d35
Registration Details
Taiwan FDA Registration: 8d9fbef5cce71165712d4bbae14a1d35
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Device Details

“ERBE” Bipolar Forceps
TW: “艾柏”雙極電燒鑷子
Risk Class 2
MD

Registration Details

8d9fbef5cce71165712d4bbae14a1d35

Ministry of Health Medical Device Import No. 031923

DHA05603192301

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 12, 2018

Dec 12, 2028