"Carestream" Radiographic Intensifying Screen (Non-Sterile) - Taiwan Registration c18dbb19ddf483b6fba3be0bc03fc4f9
Access comprehensive regulatory information for "Carestream" Radiographic Intensifying Screen (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c18dbb19ddf483b6fba3be0bc03fc4f9 and manufactured by CARESTREAM HEALTH, INC.. The authorized representative in Taiwan is FAITH BIOMED LTD..
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Device Details
Registration Details
c18dbb19ddf483b6fba3be0bc03fc4f9
Ministry of Health Medical Device Import No. 017790
DHA09401779004
Product Details
Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Radiation Enhanced Screen (P.1960)".
P Devices for radiology
P1960 Radiation Enhancement Screen
Imported from abroad
Dates and Status
May 04, 2017
May 04, 2022