Taiwan FDA registration 0af44ea251cef0b76281f47e1e261248
"Shimadzu" digital imaging system
TW: "島津"數位式影像系統
Taiwan·Risk Class 2·SHIMADZU CORPORATION, SANJO FACTORY·Registered Nov 13, 2006 – Nov 13, 2016CancelledRegistration details
- Analysis ID
- 0af44ea251cef0b76281f47e1e261248
- Customs Code
- DHA00601742701
Company information
- Manufacturer
- SHIMADZU CORPORATION, SANJO FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- SAN KWANG INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.2050 Medical image management and processing systems
- Import Information
- import
Dates and status
- Registration Date
- Nov 13, 2006
- Expiry Date
- Nov 13, 2016
- Cancellation Date
- May 10, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Shimadzu" digital imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0af44ea251cef0b76281f47e1e261248 and manufactured by SHIMADZU CORPORATION, SANJO FACTORY. The authorized representative in Taiwan is SAN KWANG INSTRUMENTS CO., LTD..
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