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“ERBE” Flexible Cryo Probe - Taiwan Registration 00f066cb185b149c5d1bfab81d1a7313

Access comprehensive regulatory information for “ERBE” Flexible Cryo Probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 00f066cb185b149c5d1bfab81d1a7313 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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00f066cb185b149c5d1bfab81d1a7313
Registration Details
Taiwan FDA Registration: 00f066cb185b149c5d1bfab81d1a7313
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Device Details

“ERBE” Flexible Cryo Probe
TW: “艾柏”軟式冷凍探針
Risk Class 2
MD

Registration Details

00f066cb185b149c5d1bfab81d1a7313

Ministry of Health Medical Device Import No. 030040

DHA05603004009

Company Information

Germany

Product Details

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

I General and plastic surgical devices

I4350 Cryosurgery equipment and accessories

Imported from abroad

Dates and Status

Aug 02, 2017

Aug 02, 2027