Taiwan FDA registration 9872e7e44705b1ef7313077166b0db36

"Cottman" ventricle cannula (unsterilized)

TW: "柯特曼"腦室套管(未滅菌)

Taiwan·Risk Class 1·Integra LifeSciences Production Corporation·Registered Apr 14, 2011 – Apr 14, 2026Expired

Registration details

Analysis ID: 9872e7e44705b1ef7313077166b0db36
Customs Code: DHA04401019208

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 "Ventricular Cannula (K.4060)" of the Classification and Grading Management Measures for Medical Devices.
Product Type (Level 1): K Neuroscience
Product Type (Level 2): K.4060 Cerebral cannula
Import Information: import

Dates and status

Registration Date: Apr 14, 2011
Expiry Date: Apr 14, 2026

About this record

Access comprehensive regulatory information for "Cottman" ventricle cannula (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9872e7e44705b1ef7313077166b0db36 and manufactured by Integra LifeSciences Production Corporation. The authorized representative in Taiwan is K&C MEDICAL 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.