Hexapole state selection and orientation of parent molecules is combined with two-dimensional ion imaging of photofragments to study the direct photolysis of deuterated methyl iodide molecules (CD 3 I) at 266 nm. The combination of these two techniques allows us to create an essentially single quantum state-selected beam of oriented molecules, which are subsequently photodissociated, and to measure the final state-, velocity-, and angle-resolved recoil distribution of the photofragments. Extensive measurements have been done on the variation of the recoil distribution with the orientation field strength applied. These measurements allow a quantitative comparison of the orientation distribution of state-selected methyl iodide molecules with theoretical Stark effect calculations. For the prompt dissociation of CD 3 I at 266 nm the angular recoil distribution of the I( 2 P 1/2 ) photofragment reflects predominantly the initial spatial orientation of the stateselected parent. A comparison is presented between the fragment recoil distributions when different initial oriented parent states are selected.