"Dangli" diagnostic X-ray tube sleeve assembly (unsterilized)
- Analysis ID
- 15537f47dd4e3bb135a710d480edec10
- Customs Code
- DHAS9401379900
- Manufacturer
- DUNLEE, A DIVISION OF PHILIPS HEALTHCARE
- Manufacturer Country
- United States
- Authorized Representative
- DR. MEDICOM CO., LTD.
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Devices "X-ray Tube Sleeve Components for Diagnosis (P.1760)".
- 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
- Jan 22, 2014
- Expiry Date
- Jan 22, 2019
- Cancellation Date
- Aug 05, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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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 15537f47dd4e3bb135a710d480edec10 and manufactured by DUNLEE, A DIVISION OF PHILIPS HEALTHCARE. The authorized representative in Taiwan is DR. MEDICOM CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including DUNLEE, A DIVISION OF PHILIPS MEDICAL SYSTEMS, CLEVELAND, INC, DUNLEE, 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.