Large sterilization - Taiwan Registration d36eed49ccde497e7a734c5ecc36c7e5
Access comprehensive regulatory information for Large sterilization in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d36eed49ccde497e7a734c5ecc36c7e5 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.
Device Details
Registration Details
d36eed49ccde497e7a734c5ecc36c7e5
DHY04300057106
Product Details
It is used for the pre-washing and decontamination of non-hazardous medical devices and equipment surfaces, and for the final sterilization or high disinfection of dangerous or semi-dangerous medical devices.
J General hospital and personal use equipment
Domestic
Dates and Status
Oct 31, 2005
Oct 31, 2010
Nov 23, 2012
Cancellation Information
Logged out
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