Taiwan FDA registration 45d4038cf52a528f9e9ae5e41c962ed5
"RUHOF" Liquizime Instrument Cleaner (Non-Sterile)
TW: "羅福" 立可奈醫療器械清潔劑 (未滅菌)
Taiwan·Risk Class 1·MD·THE RUHOF CORPORATION·Registered Sep 24, 2015 – Sep 24, 2025ExpiredRegistration details
- Analysis ID
- 45d4038cf52a528f9e9ae5e41c962ed5
- License Form
- Ministry of Health Medical Device Import No. 015694
- Customs Code
- DHA09401569401
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
- Sep 24, 2015
- Expiry Date
- Sep 24, 2025
About this record
Access comprehensive regulatory information for "RUHOF" Liquizime Instrument Cleaner (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 45d4038cf52a528f9e9ae5e41c962ed5 and manufactured by THE RUHOF CORPORATION. The authorized representative in Taiwan is HONYOU DEVELOPMENT CO., LTD..
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