Taiwan FDA registration ce19879a66416f9b27a93aeb707a1500
“FUJIFILM” COMPUTED RADIOGRAPHY XG5000 PLUS
TW: “富士”電腦X光影像讀取儀
Taiwan·Risk Class 2·MD·FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE·Registered Aug 28, 2014 – Aug 28, 2019CancelledRegistration details
- Analysis ID
- ce19879a66416f9b27a93aeb707a1500
- License Form
- Ministry of Health Medical Device Import No. 026454
- Customs Code
- DHA05602645408
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- NAN KAI CORPORATION
Product details
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1650 fluoroscopic X-ray image intensifier
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 28, 2014
- Expiry Date
- Aug 28, 2019
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “FUJIFILM” COMPUTED RADIOGRAPHY XG5000 PLUS in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ce19879a66416f9b27a93aeb707a1500 and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is NAN KAI CORPORATION.
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