Taiwan FDA registration 41fc6f4bdde60d328a1ce40170cf4026
“Xpure” Medical Surface disinfectant (Non-Sterile)
TW: “旭諾” 醫用表面殺菌噴霧 (未滅菌)
Taiwan·Risk Class 1·MD·SHINEO TECHNOLOGY CO., LTD.·Registered Oct 19, 2020 – Oct 19, 2025ExpiredRegistration details
- Analysis ID
- 41fc6f4bdde60d328a1ce40170cf4026
- License Form
- Ministry of Health Medical Device Manufacturing No. 008643
Company information
- Manufacturer
- SHINEO TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SHINEO TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration 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)
- J6890 Disinfectants for general medical devices
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 19, 2020
- Expiry Date
- Oct 19, 2025
About this record
Access comprehensive regulatory information for “Xpure” Medical Surface disinfectant (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 41fc6f4bdde60d328a1ce40170cf4026 and manufactured by SHINEO TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SHINEO TECHNOLOGY CO., LTD..
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