Taiwan FDA registration 1f25682bd1eae6ad91fc8da3b0a3f446

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

TW: "當麗" 診斷用X光球管套組件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·DUNLEE, A DIVISION OF PHILIPS MEDICAL SYSTEMS, CLEVELAND, INC·Registered May 30, 2014 – May 30, 2024Expired
Registration details
Analysis ID
1f25682bd1eae6ad91fc8da3b0a3f446
Customs Code
DHAS9401419700
Company information
Manufacturer Country
United States
Authorized Representative
UNISON COMPANY 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
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
May 30, 2014
Expiry Date
May 30, 2024
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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 1f25682bd1eae6ad91fc8da3b0a3f446 and manufactured by DUNLEE, A DIVISION OF PHILIPS MEDICAL SYSTEMS, CLEVELAND, INC. The authorized representative in Taiwan is UNISON COMPANY 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.

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