Taiwan FDA registration 20405a2677fcb51bdac1c8a207c6c0d1
Fujifilm medical three-piece box dry laser imager and its accessories
TW: 富士醫用三片箱型乾式雷射影像儀及其配件
Taiwan·Risk Class 2·FUJIFILM TECHNO PRODUCTS CO., LTD. TOUHOKU FACTORY HANAMAKI SITE·Registered Nov 22, 2005 – Nov 22, 2015CancelledRegistration details
- Analysis ID
- 20405a2677fcb51bdac1c8a207c6c0d1
- Customs Code
- DHA00601362202
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- NAN KAI CORPORATION
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.2040 醫學影像列印裝置
- Import Information
- import
Dates and status
- Registration Date
- Nov 22, 2005
- Expiry Date
- Nov 22, 2015
- Cancellation Date
- Jun 08, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Fujifilm medical three-piece box dry laser imager and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 20405a2677fcb51bdac1c8a207c6c0d1 and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOUHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is NAN KAI CORPORATION.
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