Taiwan FDA registration 22fb95f8c8ffa289a94045a796062455
"Dikang" X-ray system
TW: “帝康”X光系統
Taiwan·Risk Class 2·DK MEDICAL SYSTEMS CO., LTD.·Registered Jan 28, 2016 – Jan 28, 2026ExpiredRegistration details
- Analysis ID
- 22fb95f8c8ffa289a94045a796062455
- Customs Code
- DHAS5602816009
Company information
- Manufacturer
- DK MEDICAL SYSTEMS CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- FONN CHANG TRADING 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
- Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
- Registration Date
- Jan 28, 2016
- Expiry Date
- Jan 28, 2026
About this record
Access comprehensive regulatory information for "Dikang" X-ray system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 22fb95f8c8ffa289a94045a796062455 and manufactured by DK MEDICAL SYSTEMS CO., LTD.. The authorized representative in Taiwan is FONN CHANG TRADING CO., LTD..
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