Taiwan FDA registration 7d7506bbc238835d80721e93c49b3ae4
“RUHOF” General purpose disinfectants (Non-Sterile)
TW: “羅福”一般醫療器械用消毒劑(未滅菌)
Taiwan·Risk Class 1·MD·THE RUHOF CORPORATION·Registered Apr 29, 2019 – Apr 29, 2024ExpiredRegistration details
- Analysis ID
- 7d7506bbc238835d80721e93c49b3ae4
- License Form
- Ministry of Health Medical Device Import No. 020380
- Customs Code
- DHA09402038008
Company information
- Manufacturer
- THE RUHOF CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- HONYOU DEVELOPMENT 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
- Imported from abroad
Dates and status
- Registration Date
- Apr 29, 2019
- Expiry Date
- Apr 29, 2024
About this record
Access comprehensive regulatory information for “RUHOF” General purpose disinfectants (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 7d7506bbc238835d80721e93c49b3ae4 and manufactured by THE RUHOF CORPORATION. The authorized representative in Taiwan is HONYOU DEVELOPMENT CO., LTD..
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