Taiwan FDA registration d36eed49ccde497e7a734c5ecc36c7e5

Large sterilization

TW: 大滅菌
Taiwan flagTaiwan·Risk Class 1·GINYORK MFG. CO., LTD.·Registered Oct 31, 2005 – Oct 31, 2010Cancelled
Registration details
Analysis ID
d36eed49ccde497e7a734c5ecc36c7e5
Customs Code
DHY04300057106
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
GINYORK MFG. CO., LTD.
Product details
Intended Use
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.
Product Type (Level 1)
J General hospital and personal use equipment
Import Information
Domestic
Dates and status
Registration Date
Oct 31, 2005
Expiry Date
Oct 31, 2010
Cancellation Date
Nov 23, 2012
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 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.

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