Taiwan FDA registration f97692d4eb3206f94177a43718d1a233

Burlanc Shunt System Implantable Devices (Sterile/Unsterile)

TW: "柏朗" 雅氏分流系統植入用器械 (滅菌/未滅菌)

Taiwan·Risk Class 1·AESCULAP AG·Registered Mar 22, 2019 – Mar 22, 2029Active

Registration details

Analysis ID: f97692d4eb3206f94177a43718d1a233
Customs Code: DHA09402022509

Company information

Manufacturer: AESCULAP AG
Manufacturer Country: Germany
Authorized Representative: B. BRAUN TAIWAN CO., LTD.

Product details

Intended Use: 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.
Product Type (Level 1): K Neuroscience
Product Type (Level 2): K.4545 分流系統植入用器械
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Mar 22, 2019
Expiry Date: Mar 22, 2029

About this record

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..

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