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Burlanc Shunt System Implantable Devices (Sterile/Unsterile) - Taiwan Registration f97692d4eb3206f94177a43718d1a233

Access comprehensive regulatory information for Burlanc Shunt System Implantable Devices (Sterile/Unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f97692d4eb3206f94177a43718d1a233 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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f97692d4eb3206f94177a43718d1a233
Registration Details
Taiwan FDA Registration: f97692d4eb3206f94177a43718d1a233
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Device Details

Burlanc Shunt System Implantable Devices (Sterile/Unsterile)
TW: "ๆŸๆœ—" ้›…ๆฐๅˆ†ๆต็ณป็ตฑๆคๅ…ฅ็”จๅ™จๆขฐ (ๆป…่Œ/ๆœชๆป…่Œ)
Risk Class 1

Registration Details

f97692d4eb3206f94177a43718d1a233

DHA09402022509

Company Information

Germany

Product Details

It is limited to the first level of identification of the "Devices for Implantation in the Shunt System (K.4545)" of the Measures for the Classification and Grading of Medical Devices.

K Neuroscience

K.4545 ๅˆ†ๆต็ณป็ตฑๆคๅ…ฅ็”จๅ™จๆขฐ

Input;; QMS/QSD

Dates and Status

Mar 22, 2019

Mar 22, 2029