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"Dior" disinfectant for general medical devices (unsterilized) - Taiwan Registration 67562dbdb53aeeec0dda65423eedad1c

Access comprehensive regulatory information for "Dior" 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 67562dbdb53aeeec0dda65423eedad1c and manufactured by DIOP GMBH & CO KG. The authorized representative in Taiwan is EJOY2 CORP..

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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67562dbdb53aeeec0dda65423eedad1c
Registration Details
Taiwan FDA Registration: 67562dbdb53aeeec0dda65423eedad1c
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Device Details

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

Registration Details

67562dbdb53aeeec0dda65423eedad1c

DHA04401297001

Company Information

Germany

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

import

Dates and Status

May 03, 2013

May 03, 2023