Large sterilization
- Analysis ID
- d36eed49ccde497e7a734c5ecc36c7e5
- Customs Code
- DHY04300057106
- Manufacturer
- GINYORK MFG. CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GINYORK MFG. CO., LTD.
- 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
- Registration Date
- Oct 31, 2005
- Expiry Date
- Oct 31, 2010
- Cancellation Date
- Nov 23, 2012
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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.