Taiwan FDA registration 5cb6a216423752367f4791c4230f6651
Shimadzu digital angiography system
TW: “島津” 數位血管攝影系統
Taiwan·Risk Class 2·Shimadzu Corporation;; SHIMADZU CORPORATION, SANJO FACTORY·Registered Apr 28, 2024 – Apr 28, 2029ActiveRegistration details
- Analysis ID
- 5cb6a216423752367f4791c4230f6651
- Customs Code
- DHAS5603697702
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- SAN KANG INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1650 透視X光影像增感管
- Import Information
- Input;; The consent of the Nuclear Safety Commission must be obtained for each import of this medical device.
Dates and status
- Registration Date
- Apr 28, 2024
- Expiry Date
- Apr 28, 2029
About this record
Access comprehensive regulatory information for Shimadzu digital angiography system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5cb6a216423752367f4791c4230f6651 and manufactured by Shimadzu Corporation;; SHIMADZU CORPORATION, SANJO FACTORY. The authorized representative in Taiwan is SAN KANG INSTRUMENTS CO., LTD..
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