Taiwan FDA registration 217ed4911f1ee95474e2f904f2ebdbab
"Fully sterilized" general medical device disinfectant (unsterilized)
TW: “全滅菌”一般醫療器械消毒劑（未滅菌）
Taiwan·Risk Class 1·GINYORK MFG. CO., LTD.·Registered May 06, 2011 – May 06, 2026ExpiredRegistration details
- Analysis ID
- 217ed4911f1ee95474e2f904f2ebdbab
Company information
- Manufacturer
- GINYORK MFG. CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GINYORK MFG. CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Classification and Grading of Medical Devices "Disinfectants for General Medical Devices (J.6890)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6890 Disinfectants for general medical equipment
- Import Information
- Domestic
Dates and status
- Registration Date
- May 06, 2011
- Expiry Date
- May 06, 2026
About this record
Access comprehensive regulatory information for "Fully sterilized" general medical device disinfectant (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 217ed4911f1ee95474e2f904f2ebdbab 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. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices