"Philips" magnetic resonance imaging system
Taiwan·Risk Class 2·Philips Healthcare (Suzhou) Co., Ltd·Registered Nov 11, 2015 – Nov 11, 2020Cancelled- Analysis ID
- c876420d35565e5d5e9de860ffe271b6
- Customs Code
- DHA09200071307
- 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.1000 磁振診斷裝置
- Import Information
- Chinese goods;; 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". input
- Registration Date
- Nov 11, 2015
- Expiry Date
- Nov 11, 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" magnetic resonance imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c876420d35565e5d5e9de860ffe271b6 and manufactured by Philips Healthcare (Suzhou) Co., Ltd. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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