Taiwan FDA registration 5cc175efaf29b03d2162fea5287df41d

"Changan" shunt system implantable device (unsterilized)

TW: “長安” 分流系統植入用器械（未滅菌）

Taiwan·Risk Class 1·WELLONG INSTRUMENTS CO., LTD.·Registered Apr 04, 2006 – Apr 04, 2026Expired

Registration details

Analysis ID: 5cc175efaf29b03d2162fea5287df41d
Customs Code: DHY04300116806

Company information

Manufacturer: WELLONG INSTRUMENTS CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: WELLONG INSTRUMENTS 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: Domestic

Dates and status

Registration Date: Apr 04, 2006
Expiry Date: Apr 04, 2026

About this record

Access comprehensive regulatory information for "Changan" shunt system implantable device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5cc175efaf29b03d2162fea5287df41d and manufactured by WELLONG INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is WELLONG INSTRUMENTS CO., LTD..

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