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“Philips” SensaVue Function Magnetic Resonance Imaging Software and accessory - Taiwan Registration d8e0d5b4438620d2da07f347cb0e765a

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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d8e0d5b4438620d2da07f347cb0e765a
Registration Details
Taiwan FDA Registration: d8e0d5b4438620d2da07f347cb0e765a
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Device Details

“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
Risk Class 2
MD

Registration Details

d8e0d5b4438620d2da07f347cb0e765a

Ministry of Health Medical Device Import No. 033973

DHA05603397300

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

P Devices for radiology

P1000 Magnetic Resonance Diagnostic Unit

Imported from abroad

Dates and Status

Oct 06, 2020

Oct 06, 2025