Taiwan FDA registration 74b43adcf2efc3ae8c8b1112317c793f
"Philips" magnetic resonance imaging system software
TW: “飛利浦”磁振影像系統軟體
Taiwan·Risk Class 2·Philips DS North America LLC·Registered May 07, 2011 – May 07, 2026ExpiredRegistration details
- Analysis ID
- 74b43adcf2efc3ae8c8b1112317c793f
- Customs Code
- DHA00602230504
Company information
- Manufacturer
- Philips DS North America LLC
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- 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
- Input;; Contract manufacturing
Dates and status
- Registration Date
- May 07, 2011
- Expiry Date
- May 07, 2026
About this record
Access comprehensive regulatory information for "Philips" magnetic resonance imaging system software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 74b43adcf2efc3ae8c8b1112317c793f and manufactured by Philips DS North America LLC. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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