"Philips" magnetic resonance imaging system
Taiwan·Risk Class 2·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Registered Jul 15, 2011 – Jul 15, 2016Cancelled- Analysis ID
- 638f3493ad9001dcd8cece30651da225
- Customs Code
- DHA00602247707
- Manufacturer
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Manufacturer Country
- Netherlands
- 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
- import
- Registration Date
- Jul 15, 2011
- Expiry Date
- Jul 15, 2016
- Cancellation Date
- Apr 25, 2018
- Status
- Logged out
- Reason
- 自行鍵入
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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 638f3493ad9001dcd8cece30651da225 and manufactured by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Philips Medical Systems Nederland B.V., Philips Healthcare (Suzhou) Co., Ltd, and 5 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.