Lumipulse G PIVKA-II Calibrators set - Taiwan Registration dd2c0a611dd6e7b75b72dae7562ea972
Access comprehensive regulatory information for Lumipulse G PIVKA-II Calibrators set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dd2c0a611dd6e7b75b72dae7562ea972 and manufactured by FUJIREBIO INC., HACHIOJI FACILITY. The authorized representative in Taiwan is Grand Marquis IVD CO., LTD..
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Device Details
Registration Details
dd2c0a611dd6e7b75b72dae7562ea972
Ministry of Health Medical Device Import No. 025898
DHA05602589800
Product Details
This product is used for the correction of prothrombin detection reagents for Pas G abnormalities.
A Clinical chemistry and clinical toxicology
A1150 calibrate
Imported from abroad
Dates and Status
Feb 20, 2014
Feb 20, 2029

