Taiwan FDA registration f3655026834a4be5f693e0eec21477f3
"Dajin" X-ray diagnostic system
TW: “達勁”X光診斷系統
Taiwan·Risk Class 2·DRGEM CORPORATION·Registered Dec 19, 2011 – Dec 19, 2021CancelledRegistration details
- Analysis ID
- f3655026834a4be5f693e0eec21477f3
- Customs Code
- DHAS0602311308
Company information
- Manufacturer
- DRGEM CORPORATION
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- WITTECH 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.1680 固定式X光系統
- 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
- Dec 19, 2011
- Expiry Date
- Dec 19, 2021
- Cancellation Date
- Aug 15, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Dajin" 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 f3655026834a4be5f693e0eec21477f3 and manufactured by DRGEM CORPORATION. The authorized representative in Taiwan is WITTECH CO., LTD..
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