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Must be sterilized - Taiwan Registration f9d726e02f677ff02a46eeb7ebe55826

Access comprehensive regulatory information for Must be sterilized in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f9d726e02f677ff02a46eeb7ebe55826 and manufactured by GINYORK MFG. CO., LTD.. The authorized representative in Taiwan is GINYORK MFG. CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GINYORK MFG. CO., LTD., and 1 recent registrations in the same category. 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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f9d726e02f677ff02a46eeb7ebe55826
Registration Details
Taiwan FDA Registration: f9d726e02f677ff02a46eeb7ebe55826
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Device Details

Must be sterilized
TW: ๅฟ…ๆป…่Œ
Risk Class 1
Cancelled

Registration Details

f9d726e02f677ff02a46eeb7ebe55826

DHY04300058800

Company Information

Taiwan, Province of China

Product Details

Biocides for non-hazardous medical devices and equipment surfaces. It is used for the final sterilization or pre-washing and decontamination of dangerous or semi-hazardous medical devices before high disinfection.

J General hospital and personal use equipment

Domestic

Dates and Status

Nov 01, 2005

Nov 01, 2010

Apr 30, 2014

Cancellation Information

Logged out

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