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“Carestream” Digital Radiography Detector - Taiwan Registration 77b93972e610cd1bbc3dd2842a85e82d

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 77b93972e610cd1bbc3dd2842a85e82d 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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77b93972e610cd1bbc3dd2842a85e82d
Registration Details
Taiwan FDA Registration: 77b93972e610cd1bbc3dd2842a85e82d
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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

77b93972e610cd1bbc3dd2842a85e82d

Ministry of Health Medical Device Import No. 030157

DHA05603015704

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

Aug 20, 2017

Aug 20, 2027

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