in the case of a product containing flurtamone, flufenacet, iodosulfuron, dimethenamid-p, picoxystrobin, fosthiazate or silthiofam as one of several active substances, where necessary, amend or withdraw the authorisation by 30 June 2005 or by the date fixed for such an amendment or withdrawal in the respective Directive or Directives which added the relevant substance or substances to Annex I to Directive 91/414/EEC, whichever is the latest."
če sredstvo vsebuje flurtamon, flufenacet, jodosulfuron, dimetenamid-p, pikoksitrobin, fostiazat ali siltiofam kot eno od več aktivnih snovi, po potrebi spremenijo ali prekličejo registracije do 30. junija 2005 ali do datuma, določenega za tako spremembo ali preklic v zadevni direktivi ali direktivah, s katerimi je vključena ustrezna snov ali snovi v Prilogo I k Direktivi 91/414/EGS, kateri koli datum je poznejši."