Taiwan FDA registration cdd7048852e8e9cc64827c397014292b
Fujifilm Digital Photography System
TW: 富士數位攝影系統
Taiwan·Risk Class 2·FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE·Registered Apr 03, 2013 – Apr 03, 2018CancelledRegistration details
- Analysis ID
- cdd7048852e8e9cc64827c397014292b
- Customs Code
- DHA00602485102
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.1650 透視X光影像增感管
- Import Information
- import
Dates and status
- Registration Date
- Apr 03, 2013
- Expiry Date
- Apr 03, 2018
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Fujifilm Digital Photography System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cdd7048852e8e9cc64827c397014292b 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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