Taiwan FDA registration b2e008bb79b5f5a715a6b07de3ca230e
Fujifilm endoscopic ultrasound probe
TW: “富士”內視鏡超音波探頭
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION·Registered Jan 17, 2023 – Jan 17, 2028ActiveRegistration details
- Analysis ID
- b2e008bb79b5f5a715a6b07de3ca230e
- Customs Code
- DHA05603608700
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)
- P Radiology Science
- Product Type (Level 2)
- P.1570 診斷用超音波轉換器
- Import Information
- import
Dates and status
- Registration Date
- Jan 17, 2023
- Expiry Date
- Jan 17, 2028
About this record
Access comprehensive regulatory information for Fujifilm endoscopic ultrasound probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b2e008bb79b5f5a715a6b07de3ca230e and manufactured by FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..
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