Taiwan FDA registration f95602b0671c4a9e0348aa91c9fb455c
Vitripei Disinfectant for general medical devices (unsterilized)
TW: 維特瑞沛 一般醫療器械用消毒液 (未滅菌)
Registration details
- Analysis ID
- f95602b0671c4a9e0348aa91c9fb455c
Company information
- Manufacturer
- ACELAB INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Berdia Biotechnology 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
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Mar 02, 2015
- Expiry Date
- Mar 02, 2025
About this record
Access comprehensive regulatory information for Vitripei 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 f95602b0671c4a9e0348aa91c9fb455c and manufactured by ACELAB INC.. The authorized representative in Taiwan is Berdia Biotechnology 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