Taiwan FDA registration 15537f47dd4e3bb135a710d480edec10

"Dangli" diagnostic X-ray tube sleeve assembly (unsterilized)

TW: "當利"診斷用X光球管套組件(未滅菌)
Taiwan flagTaiwan·Risk Class 1·DUNLEE, A DIVISION OF PHILIPS HEALTHCARE·Registered Jan 22, 2014 – Jan 22, 2019Cancelled
Registration details
Analysis ID
15537f47dd4e3bb135a710d480edec10
Customs Code
DHAS9401379900
Company information
Manufacturer Country
United States
Authorized Representative
DR. MEDICOM CO., LTD.
Product details
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
Dates and status
Registration Date
Jan 22, 2014
Expiry Date
Jan 22, 2019
Cancellation Date
Aug 05, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

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.

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