X-ray tube sleeve assembly for diagnostic "Dengli" (unsterilized)
Taiwan·Risk Class 1·DUNLEE·Registered Aug 25, 2016 – Aug 25, 2026Active- Analysis ID
- 82cfa8d1f902864488fc3d8978cfe2fa
- Customs Code
- DHA09401692802
- Manufacturer
- DUNLEE
- Manufacturer Country
- United States
- Authorized Representative
- PAN ASIA INTERNATIONAL INSTRUMENTS 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
- Aug 25, 2016
- Expiry Date
- Aug 25, 2026
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Access comprehensive regulatory information for X-ray tube sleeve assembly for diagnostic "Dengli" (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 82cfa8d1f902864488fc3d8978cfe2fa and manufactured by DUNLEE. The authorized representative in Taiwan is PAN ASIA INTERNATIONAL INSTRUMENTS CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DUNLEE, and 2 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.