"Dangli" diagnostic X-ray tube sleeve assembly (unsterilized)
Taiwan·Risk Class 1·DUNLEE·Registered Dec 21, 2016 – Dec 21, 2021Cancelled- Analysis ID
- e12949b451c6b00d145984bf648fabf9
- Customs Code
- DHAS9401731801
- Manufacturer
- DUNLEE
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- 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
- Dec 21, 2016
- Expiry Date
- Dec 21, 2021
- Cancellation Date
- Sep 08, 2023
- 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 e12949b451c6b00d145984bf648fabf9 and manufactured by DUNLEE. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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, A DIVISION OF PHILIPS HEALTHCARE, 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.