X-ray tube sleeve assembly for diagnostic "Dengli" (unsterilized)
Taiwan·Risk Class 1·DUNLEE·Registered Jun 16, 2006 – Jun 16, 2016Cancelled- Analysis ID
- 351ea237d2f383715f4800d07f80a26d
- Customs Code
- DHA04400473903
- 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 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
- Jun 16, 2006
- Expiry Date
- Jun 16, 2016
- Cancellation Date
- Jun 26, 2018
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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 351ea237d2f383715f4800d07f80a26d 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.