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“CARESTREAM” Digital Radiography Detector - Taiwan Registration 2340d9f0b0580d4ff97314a2f5b07529

Access comprehensive regulatory information for “CARESTREAM” Digital Radiography Detector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2340d9f0b0580d4ff97314a2f5b07529 and manufactured by Carestream Health, Inc.. The authorized representative in Taiwan is FAITH BIOMED LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Carestream Health, Inc., and 1 recent registrations in the same category. 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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2340d9f0b0580d4ff97314a2f5b07529
Registration Details
Taiwan FDA Registration: 2340d9f0b0580d4ff97314a2f5b07529
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Device Details

“CARESTREAM” Digital Radiography Detector
TW: “康世”數位平板X光偵測器
Risk Class 2
MD

Registration Details

2340d9f0b0580d4ff97314a2f5b07529

Ministry of Health Medical Device Import No. 029101

DHA05602910103

Company Information

United States

Product Details

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

P Devices for radiology

P1650 fluoroscopic X-ray image intensifier

Imported from abroad

Dates and Status

Nov 16, 2016

Nov 16, 2026

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