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“ERBE” APCapplicator - Taiwan Registration 8635d5bdea741ffe1051ff4032175716

Access comprehensive regulatory information for “ERBE” APCapplicator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8635d5bdea741ffe1051ff4032175716 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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8635d5bdea741ffe1051ff4032175716
Registration Details
Taiwan FDA Registration: 8635d5bdea741ffe1051ff4032175716
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Device Details

“ERBE” APCapplicator
TW: “艾柏”氬氣電漿凝固探頭
Risk Class 2
MD

Registration Details

8635d5bdea741ffe1051ff4032175716

Ministry of Health Medical Device Import No. 030577

DHA05603057700

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 05, 2017

Dec 05, 2027