"Philips" magnetic resonance imaging system
Taiwan·Risk Class 2·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Registered Jan 09, 2006 – Jan 09, 2021Cancelled- Analysis ID
- 3d8e1707a0eb430cba8e9a6ae1ed6764
- Customs Code
- DHA00601386604
- 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
- Import Information
- import
- Registration Date
- Jan 09, 2006
- Expiry Date
- Jan 09, 2021
- Cancellation Date
- Sep 08, 2023
- 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 3d8e1707a0eb430cba8e9a6ae1ed6764 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.