Taiwan FDA registration 5a70fa413eeec6b5e5a62a912abf3b97
"Fujino" ultrasound endoscope
TW: “富士能”超音波內視鏡
Taiwan·Risk Class 2·FUJINON SANO CORPORATION·Registered May 14, 2008 – May 14, 2013CancelledRegistration details
- Analysis ID
- 5a70fa413eeec6b5e5a62a912abf3b97
- Customs Code
- DHA00601885600
Company information
- Manufacturer
- FUJINON SANO CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- WELMORE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- May 14, 2008
- Expiry Date
- May 14, 2013
- Cancellation Date
- Aug 03, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Fujino" ultrasound endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5a70fa413eeec6b5e5a62a912abf3b97 and manufactured by FUJINON SANO CORPORATION. The authorized representative in Taiwan is WELMORE CO., LTD..
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