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Fujifilm medical three-piece box dry laser imager and its accessories - Taiwan Registration 20405a2677fcb51bdac1c8a207c6c0d1

Access comprehensive regulatory information for Fujifilm medical three-piece box dry laser imager and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 20405a2677fcb51bdac1c8a207c6c0d1 and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOUHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is NAN KAI CORPORATION.

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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20405a2677fcb51bdac1c8a207c6c0d1
Registration Details
Taiwan FDA Registration: 20405a2677fcb51bdac1c8a207c6c0d1
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Device Details

Fujifilm medical three-piece box dry laser imager and its accessories
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Risk Class 2
Cancelled

Registration Details

20405a2677fcb51bdac1c8a207c6c0d1

DHA00601362202

Company Information

Product Details

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

P Radiology Science

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import

Dates and Status

Nov 22, 2005

Nov 22, 2015

Jun 08, 2018

Cancellation Information

Logged out

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