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“Aesculap” Elan 4 Power Instruments and Accessories - Taiwan Registration 0427acddddccf81b9b091e6e4bebd1e4

Access comprehensive regulatory information for “Aesculap” Elan 4 Power Instruments and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0427acddddccf81b9b091e6e4bebd1e4 and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN 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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0427acddddccf81b9b091e6e4bebd1e4
Registration Details
Taiwan FDA Registration: 0427acddddccf81b9b091e6e4bebd1e4
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Device Details

“Aesculap” Elan 4 Power Instruments and Accessories
TW: “雅氏”怡然動力工具及其附件
Risk Class 2
MD

Registration Details

0427acddddccf81b9b091e6e4bebd1e4

Ministry of Health Medical Device Import No. 034725

DHA05603472509

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

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Dates and Status

Jul 24, 2021

Jul 24, 2026