Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
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Field safety notice issued to inform customers that 200904v1 allele update .Uch files on certain high resolution kits do not separate cross locus alleles string results when creating reports in unimatch v4.01. with unimatch software interpretation this causes a no typing. with manual worksheet interpretation customers are not affected and receive a correct typing.