| abstract |
A unitary tray base (10) includes a first region (20) and a second region (22) which are separated by a demarcation zone (16). Medical products (30) are received in pockets (32) of the first tray region. An ethylene oxide permeable lid portion (40) seals the first tray portion from the second tray portion and the ambient atmosphere. The tray and received medical products are sterilized with ethylene oxide or other sterilizing procedures. After the sterilization, a vial (50) of contrast agent, which cannot be present during the sterilizing, is placed in a pocket (50a) of the second tray portion. A second lid portion (52) seals the vial in the second tray portion. The lid portions are marked (60-68) to indicate that the contents of the first region are sterile and the contents of the second region are not. |