Taiwan FDA registration 871e2ec595ffef87e9213a0d7df1bfe6
Fujifilm digital X-ray image reading system and accessories thereof
TW: “富士”數位X光影像讀取系統及其配件
Taiwan·Risk Class 2·FUJIFILM TECHNO PRODUCTS CO., LTD. TOUHOKU FACTORY HANAMAKI SITE·Registered Dec 02, 2008 – Dec 02, 2013CancelledRegistration details
- Analysis ID
- 871e2ec595ffef87e9213a0d7df1bfe6
- Customs Code
- DHA00601938100
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
- Dec 02, 2008
- Expiry Date
- Dec 02, 2013
- Cancellation Date
- Jun 11, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Fujifilm digital X-ray image reading system and accessories thereof in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 871e2ec595ffef87e9213a0d7df1bfe6 and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOUHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is NAN KAI CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices