Taiwan FDA registration 4fdf10b8101e01906f5f797f459578ac
"Hitachi" digital image processing device
TW: “日立”數位影像處理裝置
Taiwan·Risk Class 2·HITACHI MEDICAL CORPORATION, MEDICAL SYSTEM OPERATIONS GROUP, KASHIWA·Registered May 03, 2011 – May 03, 2016CancelledRegistration details
- Analysis ID
- 4fdf10b8101e01906f5f797f459578ac
- Customs Code
- DHA00602229705
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- PROMED INSTRUMENT CO., LTD.
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
- May 03, 2011
- Expiry Date
- May 03, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Hitachi" digital image processing device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4fdf10b8101e01906f5f797f459578ac and manufactured by HITACHI MEDICAL CORPORATION, MEDICAL SYSTEM OPERATIONS GROUP, KASHIWA. The authorized representative in Taiwan is PROMED INSTRUMENT CO., LTD..
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