Taiwan FDA registration 40f4fe12264aa8069d5230d4070a1100

"Sterix" disinfectant for general medical devices (unsterilized)

TW: "思泰瑞" 一般醫療器械用消毒劑 (未滅菌)

Taiwan·Risk Class 1·STERIS CORPORATION·Registered Dec 02, 2016 – Dec 02, 2021Cancelled

Registration details

Analysis ID: 40f4fe12264aa8069d5230d4070a1100
Customs Code: DHA09401724709

Company information

Manufacturer: STERIS CORPORATION
Manufacturer Country: United States
Authorized Representative: CHUNG TENG MEDICAL INSTRUMENTS CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Disinfectants for General Medical Devices (J.6890)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6890 Disinfectants for general medical equipment
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Dec 02, 2016
Expiry Date: Dec 02, 2021
Cancellation Date: Sep 08, 2023

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Sterix" disinfectant for general medical devices (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 40f4fe12264aa8069d5230d4070a1100 and manufactured by STERIS CORPORATION. The authorized representative in Taiwan is CHUNG TENG MEDICAL INSTRUMENTS CO., LTD..

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