Taiwan FDA registration d8e0d5b4438620d2da07f347cb0e765a
“Philips” SensaVue Function Magnetic Resonance Imaging Software and accessory
TW: “飛利浦”麗莎芙磁振造影軟體與配件
Taiwan·Risk Class 2·MD·INVIVO CORPORATION·Registered Oct 06, 2020 – Oct 06, 2025ExpiredRegistration details
- Analysis ID
- d8e0d5b4438620d2da07f347cb0e765a
- License Form
- Ministry of Health Medical Device Import No. 033973
- Customs Code
- DHA05603397300
Company information
- Manufacturer
- INVIVO CORPORATION
- 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 Devices for radiology
- Product Type (Level 2)
- P1000 Magnetic Resonance Diagnostic Unit
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 06, 2020
- Expiry Date
- Oct 06, 2025
About this record
Access comprehensive regulatory information for “Philips” SensaVue Function Magnetic Resonance Imaging Software and accessory in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d8e0d5b4438620d2da07f347cb0e765a and manufactured by INVIVO CORPORATION. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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