Taiwan FDA registration 4bc3e802a17131e9c009dc922665b03c

"ANEXI" disinfectant for general medical devices (unsterilized)

TW: “安能適” 一般醫療器械用消毒劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·ANIOS LABORATORIES·Registered May 20, 2020 – May 20, 2030Active
Registration details
Analysis ID
4bc3e802a17131e9c009dc922665b03c
Customs Code
DHA09402155002
Company information
Manufacturer
ANIOS LABORATORIES
Manufacturer Country
France
Authorized Representative
Yida Industrial Co., Ltd
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Classification and Grading 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
QMS/QSD;; 輸入
Dates and status
Registration Date
May 20, 2020
Expiry Date
May 20, 2030
About this record

Access comprehensive regulatory information for "ANEXI" 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 4bc3e802a17131e9c009dc922665b03c and manufactured by ANIOS LABORATORIES. The authorized representative in Taiwan is Yida Industrial 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 DatabasePowered by Pure Global AI89,000+ Devices