Taiwan FDA registration 4e45f53aa0002030172d139ceae09328
"Qi Yi Mead" X-ray tube sleeve assembly for diagnosis (unsterilized)
TW: "齊翌美德" 診斷用X光球管套組件(未滅菌)
Taiwan·Risk Class 1·GE MEDICAL SYSTEMS S.A.·Registered Jul 14, 2020 – Jul 14, 2025ExpiredRegistration details
- Analysis ID
- 4e45f53aa0002030172d139ceae09328
- Customs Code
- DHAS9402173901
Company information
- Manufacturer
- GE MEDICAL SYSTEMS S.A.
- Manufacturer Country
- France
- Authorized Representative
- DR. MEDICOM CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "X-ray tube sleeve assembly for diagnosis (P.1760)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1760 診斷用X光球管套組件
- 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
- Jul 14, 2020
- Expiry Date
- Jul 14, 2025
About this record
Access comprehensive regulatory information for "Qi Yi Mead" X-ray tube sleeve assembly for diagnosis (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4e45f53aa0002030172d139ceae09328 and manufactured by GE MEDICAL SYSTEMS S.A.. The authorized representative in Taiwan is DR. MEDICOM CO., LTD..
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