Pure Global

"Sterix" disinfectant for general medical devices (unsterilized) - Taiwan Registration 40f4fe12264aa8069d5230d4070a1100

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..

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
40f4fe12264aa8069d5230d4070a1100
Registration Details
Taiwan FDA Registration: 40f4fe12264aa8069d5230d4070a1100
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Sterix" disinfectant for general medical devices (unsterilized)
TW: "ๆ€ๆณฐ็‘ž" ไธ€่ˆฌ้†ซ็™‚ๅ™จๆขฐ็”จๆถˆๆฏ’ๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

40f4fe12264aa8069d5230d4070a1100

DHA09401724709

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Disinfectants for General Medical Devices (J.6890)".

J General hospital and personal use equipment

J.6890 Disinfectants for general medical equipment

Input;; QMS/QSD

Dates and Status

Dec 02, 2016

Dec 02, 2021

Sep 08, 2023

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€