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Software for "Invivo" magnetic resonance diagnostic device - Taiwan Registration 39ff093f8ed299619d61ad9cca90a687

Access comprehensive regulatory information for Software for "Invivo" magnetic resonance diagnostic device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 39ff093f8ed299619d61ad9cca90a687 and manufactured by INVIVO CORPORATION INC.. The authorized representative in Taiwan is Bowex GmbH.

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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39ff093f8ed299619d61ad9cca90a687
Registration Details
Taiwan FDA Registration: 39ff093f8ed299619d61ad9cca90a687
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Device Details

Software for "Invivo" magnetic resonance diagnostic device
TW: โ€œ่‹ฑ็ถญๆฒƒโ€็ฃๆŒฏ่จบๆ–ท่ฃ็ฝฎ็”จ่ปŸ้ซ”
Risk Class 2
Cancelled

Registration Details

39ff093f8ed299619d61ad9cca90a687

DHA00601805607

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

May 07, 2007

May 07, 2012

May 05, 2014

Cancellation Information

Logged out

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