Commission Directive 2005/61/ECDangos y teitl llawn

Commission Directive 2005/61/EC of 30 September 2005 implementing Directive 2002/98/EC of the European Parliament and of the Council as regards traceability requirements and notification of serious adverse reactions and events (Text with EEA relevance)

BY FACILITIES

1.Blood component supplier identification

2.Issued blood component identification

3.Transfused recipient identification

4.For blood units not transfused, confirmation of subsequent disposition

5.Date of transfusion or disposition (year/month/day)

6.Lot number of the component, if relevant.