"Philips" computed tomography diagnostic device
Taiwan·Risk Class 2·Philips Healthcare (Suzhou) Co., Ltd·Registered Dec 11, 2014 – Mar 25, 2024Cancelled- Analysis ID
- 23addef40caa63d22099d7c5b1c6baab
- Customs Code
- DHAS9200063903
- Manufacturer
- Philips Healthcare (Suzhou) Co., Ltd
- Manufacturer Country
- China
- 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
- Input;; 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 letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
- Registration Date
- Dec 11, 2014
- Expiry Date
- Mar 25, 2024
- Cancellation Date
- Sep 10, 2020
- Status
- Logged out
- Reason
- 自請註銷
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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 23addef40caa63d22099d7c5b1c6baab and manufactured by Philips Healthcare (Suzhou) Co., Ltd. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC., PHILIPS MEDICAL SYSTEM TECHNOLOGIES LTD., 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.