Taiwan FDA registration e62ed572b0a7053a4c1d632869918567
"Shimadzu" image intensifier
TW: "島津" 影像增強器
Taiwan·Risk Class 2·SHIMADZU CORPORATION, SANJO FACTORY·Registered Nov 07, 2005 – Nov 07, 2015CancelledRegistration details
- Analysis ID
- e62ed572b0a7053a4c1d632869918567
- Customs Code
- DHA00601296106
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
- Import Information
- import
Dates and status
- Registration Date
- Nov 07, 2005
- Expiry Date
- Nov 07, 2015
- 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" image intensifier in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e62ed572b0a7053a4c1d632869918567 and manufactured by SHIMADZU CORPORATION, SANJO FACTORY. The authorized representative in Taiwan is SAN KWANG INSTRUMENTS CO., LTD..
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