Pure Global

“Aesculap” Elan 4Pneumatic System - Taiwan Registration fdb90eaee2a49fa2d1562786e2671d9e

Access comprehensive regulatory information for “Aesculap” Elan 4Pneumatic System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fdb90eaee2a49fa2d1562786e2671d9e 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
fdb90eaee2a49fa2d1562786e2671d9e
Registration Details
Taiwan FDA Registration: fdb90eaee2a49fa2d1562786e2671d9e
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Aesculap” Elan 4Pneumatic System
TW: “雅氏”怡然氣動工具系統
Risk Class 2
MD

Registration Details

fdb90eaee2a49fa2d1562786e2671d9e

Ministry of Health Medical Device Import No. 032695

DHA05603269503

Company Information

Germany

Product Details

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

K Devices for neuroscience

K4370 Pneumatic Head Cranial Drill Motor

Imported from abroad

Dates and Status

Jun 22, 2019

Jun 22, 2024