Taiwan FDA registration 13ce3a284205a9bcf2eccac9b2ec0911
"Quanpeng" general medical device disinfectant (unsterilized)
TW: "全鵬"一般醫療器械用消毒劑(未滅菌)
Taiwan·Risk Class 1·Zhudong Factory of Huanbo Technology Co., Ltd·Registered Jun 14, 2013 – Jun 14, 2028ActiveRegistration details
- Analysis ID
- 13ce3a284205a9bcf2eccac9b2ec0911
Company information
- Manufacturer
- Zhudong Factory of Huanbo Technology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ATK ALLWAYS TECHNOLOGY CORP.
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;; Contract manufacturing
Dates and status
- Registration Date
- Jun 14, 2013
- Expiry Date
- Jun 14, 2028
About this record
Access comprehensive regulatory information for "Quanpeng" 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 13ce3a284205a9bcf2eccac9b2ec0911 and manufactured by Zhudong Factory of Huanbo Technology Co., Ltd. The authorized representative in Taiwan is ATK ALLWAYS TECHNOLOGY CORP..
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