Taiwan FDA registration 24aec3a4e5ee1d639f7c71da89d5d11d
General sterilization Disinfectant for general medical devices (unsterilized)
TW: 普滅菌 一般醫療器械用消毒劑(未滅菌)
Registration details
- Analysis ID
- 24aec3a4e5ee1d639f7c71da89d5d11d
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
- Mar 01, 2011
- Expiry Date
- Mar 01, 2026
About this record
Access comprehensive regulatory information for General sterilization Disinfectant for general medical devices (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 24aec3a4e5ee1d639f7c71da89d5d11d 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