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Philips magnetic resonance imaging software system - Taiwan Registration aa47c8c99cd12fb42b17213e856595f3

Access comprehensive regulatory information for Philips magnetic resonance imaging software system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aa47c8c99cd12fb42b17213e856595f3 and manufactured by INVIVO CORPORATION. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details. 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.

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aa47c8c99cd12fb42b17213e856595f3
Registration Details
Taiwan FDA Registration: aa47c8c99cd12fb42b17213e856595f3
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Device Details

Philips magnetic resonance imaging software system
TW: ้ฃ›ๅˆฉๆตฆ็ฃๆŒฏ้€ ๅฝฑ่ปŸ้ซ”็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

aa47c8c99cd12fb42b17213e856595f3

DHA00602158301

Company Information

United States

Product Details

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

P Radiology Science

P.1000 ็ฃๆŒฏ่จบๆ–ท่ฃ็ฝฎ

import

Dates and Status

Oct 18, 2010

Oct 18, 2015

Apr 25, 2018

Cancellation Information

Logged out

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