"Philips" computed tomography diagnostic device
Taiwan·Risk Class 2·PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC.·Registered Nov 23, 2010 – Nov 23, 2020Cancelled- Analysis ID
- 324f333a90f3b6f76105e333d323edeb
- Customs Code
- DHAS0602172707
- Manufacturer
- PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC.
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1750 電腦斷層掃描X光系統
- Import Information
- The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
- Registration Date
- Nov 23, 2010
- Expiry Date
- Nov 23, 2020
- Cancellation Date
- Jul 15, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for "Philips" computed tomography diagnostic device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 324f333a90f3b6f76105e333d323edeb and manufactured by PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including Philips Healthcare (Suzhou) Co., Ltd, 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.