Taiwan FDA registration 44810b5fe7759f6cb96515c1a3ec6a05
"Shimadzu" X-ray diagnostic system
TW: “島津”X光透視診斷系統
Taiwan·Risk Class 2·SHIMADZU CORPORATION, SANJO FACTORY·Registered Sep 30, 2009 – Sep 30, 2019CancelledRegistration details
- Analysis ID
- 44810b5fe7759f6cb96515c1a3ec6a05
- Customs Code
- DHAS0602021208
Company information
- Manufacturer
- SHIMADZU CORPORATION, SANJO FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- SAN KANG INSTRUMENTS 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.1660 非透視X光影像增感管
- Import Information
- Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
Dates and status
- Registration Date
- Sep 30, 2009
- Expiry Date
- Sep 30, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Shimadzu" X-ray diagnostic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 44810b5fe7759f6cb96515c1a3ec6a05 and manufactured by SHIMADZU CORPORATION, SANJO FACTORY. The authorized representative in Taiwan is SAN KANG INSTRUMENTS CO., LTD..
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