"Dangli" diagnostic X-ray tube sleeve assembly (unsterilized)
Taiwan·Risk Class 1·DUNLEE, A DIVISION OF PHILIPS MEDICAL SYSTEMS, CLEVELAND, INC·Registered May 30, 2014 – May 30, 2024Expired- Analysis ID
- 6379476e100e17fde1f3142cc71583ee
- Customs Code
- DHAS9401419601
- Manufacturer Country
- United States
- Authorized Representative
- PROMEDICS TECHNOLOGY CO., LTD.
- 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); input
- Registration Date
- May 30, 2014
- Expiry Date
- May 30, 2024
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Access comprehensive regulatory information for "Dangli" 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 6379476e100e17fde1f3142cc71583ee and manufactured by DUNLEE, A DIVISION OF PHILIPS MEDICAL SYSTEMS, CLEVELAND, INC. The authorized representative in Taiwan is PROMEDICS TECHNOLOGY CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including DUNLEE, DUNLEE, A DIVISION OF PHILIPS MEDICAL SYSTEMS, CLEVELAND, INC, and 3 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.