Taiwan FDA registration 3c8e0f6c47f2b733b0b63e76fa93579f
"RDA" diagnostic X-ray tube sleeve assembly (unsterilized)
TW: "銳迪" 診斷用X光球管套組件(未滅菌)
Taiwan·Risk Class 1·HANGZHOU KAILONG MEDICAL INSTRUMENTS CO., LTD.·Registered Jun 10, 2019 – Jun 10, 2029ActiveRegistration details
- Analysis ID
- 3c8e0f6c47f2b733b0b63e76fa93579f
- Customs Code
- DHAS9600383205
Company information
- Manufacturer
- HANGZHOU KAILONG MEDICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- PO YE X-RAY MFG. CORP.
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
- Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); Chinese goods;; input
Dates and status
- Registration Date
- Jun 10, 2019
- Expiry Date
- Jun 10, 2029
About this record
Access comprehensive regulatory information for "RDA" diagnostic X-ray tube sleeve assembly (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3c8e0f6c47f2b733b0b63e76fa93579f and manufactured by HANGZHOU KAILONG MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is PO YE X-RAY MFG. CORP..
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