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Vitripei Disinfectant for general medical devices (unsterilized) - Taiwan Registration f95602b0671c4a9e0348aa91c9fb455c

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.

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f95602b0671c4a9e0348aa91c9fb455c
Registration Details
Taiwan FDA Registration: f95602b0671c4a9e0348aa91c9fb455c
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Device Details

Vitripei Disinfectant for general medical devices (unsterilized)
TW: ็ถญ็‰น็‘žๆฒ› ไธ€่ˆฌ้†ซ็™‚ๅ™จๆขฐ็”จๆถˆๆฏ’ๆถฒ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

f95602b0671c4a9e0348aa91c9fb455c

Company Information

Taiwan, Province of China

Product Details

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)".

J General hospital and personal use equipment

J.6890 Disinfectants for general medical equipment

Domestic;; Contract manufacturing

Dates and Status

Mar 02, 2015

Mar 02, 2025