Taiwan FDA registration ca7f77f3d1e290f90ba53de509260bf8

Implantable Devices for the Cottman Shunt System (Unsterilized)

TW: 〝柯特曼〞分流系統植入用器械 (未滅菌)

Taiwan·Risk Class 1·Integra LifeSciences Production Corporation·Registered Nov 25, 2010 – Nov 25, 2025Expired

Registration details

Analysis ID: ca7f77f3d1e290f90ba53de509260bf8
Customs Code: DHA04400958501

Company information

Manufacturer: Integra LifeSciences Production Corporation
Manufacturer Country: United States
Authorized Representative: K&C MEDICAL 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: import

Dates and status

Registration Date: Nov 25, 2010
Expiry Date: Nov 25, 2025

About this record

Access comprehensive regulatory information for Implantable Devices for the Cottman Shunt System (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ca7f77f3d1e290f90ba53de509260bf8 and manufactured by Integra LifeSciences Production Corporation. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..

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