Taiwan FDA registration f9d726e02f677ff02a46eeb7ebe55826

Must be sterilized

TW: 必滅菌
Taiwan flagTaiwan·Risk Class 1·GINYORK MFG. CO., LTD.·Registered Nov 01, 2005 – Nov 01, 2010Cancelled
Registration details
Analysis ID
f9d726e02f677ff02a46eeb7ebe55826
Customs Code
DHY04300058800
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
GINYORK MFG. CO., LTD.
Product details
Intended Use
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.
Product Type (Level 1)
J General hospital and personal use equipment
Import Information
Domestic
Dates and status
Registration Date
Nov 01, 2005
Expiry Date
Nov 01, 2010
Cancellation Date
Apr 30, 2014
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

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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