Taiwan FDA registration 02d73a03ee1eb8a89aed1d1c350afc1c
"Rofo" Ndonai Bomi Medical Device Cleaner (Unsterilized)
TW: “羅福”恩多奈博美醫療器械清潔劑 (未滅菌)
Registration details
- Analysis ID
- 02d73a03ee1eb8a89aed1d1c350afc1c
- Customs Code
- DHA04400785102
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 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
- import
Dates and status
- Registration Date
- Jun 25, 2009
- Expiry Date
- Jun 25, 2029
About this record
Access comprehensive regulatory information for "Rofo" Ndonai Bomi Medical Device Cleaner (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 02d73a03ee1eb8a89aed1d1c350afc1c and manufactured by THE RUHOF CORPORATION. The authorized representative in Taiwan is HONYOU DEVELOPMENT CO., LTD..
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