Taiwan FDA registration c03ba0e02799cb544988e2027f25ffe7
"Fujifilm" endoscope cleaning machine
TW: “富士”內視鏡清洗機
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION·Registered Sep 05, 2023 – Sep 05, 2028ActiveRegistration details
- Analysis ID
- c03ba0e02799cb544988e2027f25ffe7
- Customs Code
- DHA05603671707
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- FUJIFILM HEALTHCARE TAIWAN CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6992 醫用清洗消毒器
- Import Information
- import
Dates and status
- Registration Date
- Sep 05, 2023
- Expiry Date
- Sep 05, 2028
About this record
Access comprehensive regulatory information for "Fujifilm" endoscope cleaning machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c03ba0e02799cb544988e2027f25ffe7 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..
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