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“B. Braun” Aesculap Electrosurgical System - Taiwan Registration 0e3111117356dedd8ebb571414f74d84

Access comprehensive regulatory information for “B. Braun” Aesculap Electrosurgical System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0e3111117356dedd8ebb571414f74d84 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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0e3111117356dedd8ebb571414f74d84
Registration Details
Taiwan FDA Registration: 0e3111117356dedd8ebb571414f74d84
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Device Details

“B. Braun” Aesculap Electrosurgical System
TW: “柏朗”雅氏雙極電燒系統
Risk Class 2
MD

Registration Details

0e3111117356dedd8ebb571414f74d84

Ministry of Health Medical Device Import No. 035588

DHA05603558804

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4400 Electric knife for cutting and hemostasis and its accessories

Imported from abroad

Dates and Status

Jun 29, 2022

Jun 29, 2027