Taiwan FDA registration ff9e070b9a260b90dffc0b0dec7b2dc0
“RUHOF” Prepzyme Forever Wet (Non-Sterile)
TW: “羅福” 器械運輸保濕預清洗劑 (未滅菌)
Taiwan·Risk Class 1·MD·THE RUHOF CORPORATION·Registered Aug 16, 2018 – Aug 16, 2028ActiveRegistration details
- Analysis ID
- ff9e070b9a260b90dffc0b0dec7b2dc0
- License Form
- Ministry of Health Medical Device Import No. 019505
- Customs Code
- DHA09401950502
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
- Aug 16, 2018
- Expiry Date
- Aug 16, 2028
About this record
Access comprehensive regulatory information for “RUHOF” Prepzyme Forever Wet (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 ff9e070b9a260b90dffc0b0dec7b2dc0 and manufactured by THE RUHOF CORPORATION. The authorized representative in Taiwan is HONYOU DEVELOPMENT CO., LTD..
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