Taiwan FDA registration 25a4714e78f1e9771d90e8b1f2a0e54a

"Clex" non-powered neurosurgical instruments (unsterilized)

TW: “柯勒仕”非動力式神經外科用器械 (未滅菌)

Taiwan·Risk Class 1·KOROS USA, INC.·Registered May 17, 2006 – May 17, 2021Cancelled

Registration details

Analysis ID: 25a4714e78f1e9771d90e8b1f2a0e54a
Customs Code: DHA04400450402

Company information

Manufacturer: KOROS USA, INC.
Manufacturer Country: United States
Authorized Representative: MYWAY INTERNATIONAL CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Neurosurgical Devices (K.4535)".
Product Type (Level 1): K Neuroscience
Product Type (Level 2): K.4535 非動力式神經外科用器械
Import Information: import

Dates and status

Registration Date: May 17, 2006
Expiry Date: May 17, 2021
Cancellation Date: Jun 22, 2020

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for "Clex" non-powered neurosurgical instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 25a4714e78f1e9771d90e8b1f2a0e54a and manufactured by KOROS USA, INC.. The authorized representative in Taiwan is MYWAY INTERNATIONAL 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.