Taiwan FDA registration 77b93972e610cd1bbc3dd2842a85e82d

“Carestream” Digital Radiography Detector

TW: “康世”數位平板X光偵測器
Taiwan flagTaiwan·Risk Class 2·MD·Carestream Health, Inc.·Registered Aug 20, 2017 – Aug 20, 2027Active
Registration details
Analysis ID
77b93972e610cd1bbc3dd2842a85e82d
License Form
Ministry of Health Medical Device Import No. 030157
Customs Code
DHA05603015704
Company information
Manufacturer Country
United States
Authorized Representative
FAITH BIOMED LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
P Devices for radiology
Product Type (Level 2)
P1650 fluoroscopic X-ray image intensifier
Import Information
Imported from abroad
Dates and status
Registration Date
Aug 20, 2017
Expiry Date
Aug 20, 2027
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About this record

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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