A donated blood collection kit includes an easy-to-open closed container. Stored within the container are items necessary or useful for collecting donated blood, such as an antiseptic scrub, an antiseptic swab, test tubes, a blood collection container, a gauze pad and a sheet of pre-printed adhesive
A donated blood collection kit includes an easy-to-open closed container. Stored within the container are items necessary or useful for collecting donated blood, such as an antiseptic scrub, an antiseptic swab, test tubes, a blood collection container, a gauze pad and a sheet of pre-printed adhesive barcode labels. Each kit is assigned a unique identification when the kit is manufactured. The identification may eventually be used as the unique donor identification for a unit of donated blood that is collected using the items in the kit. The container is pre-labeled with the unique identification, such as by a barcode or an RF-ID tag. The test tubes and, if included, the blood collection container are pre-labeled with the same unique donor identification. The adhesive barcode labels in the container are pre-printed with the same unique donor identification and may be affixed to items that are not provided in the kit but, nonetheless, should be associated with the unit of blood that may be collected using the kit. Information about lot numbers and expiration dates for the items in the kit may be encoded in the kit's unique identification and/or stored in a database in association with the kit's identification.
대표청구항▼
1. A system for facilitating collecting donated blood, the system comprising: a plurality of kits, each kit comprising a closed container having a computer-readable representation of data including a unique identification of the kit, the container having disposed therewithin: at least one sealed tes
1. A system for facilitating collecting donated blood, the system comprising: a plurality of kits, each kit comprising a closed container having a computer-readable representation of data including a unique identification of the kit, the container having disposed therewithin: at least one sealed test tube, devoid of any blood product, having a computer-readable representation of data including the unique identification of the kit and an expiration date of the test tube; anda release sheet substrate having a plurality of adhesive labels releasably attached thereto, each of the plurality of adhesive labels having a computer-readable representation of data including the unique identification of the kit; anda computerized database storing, for each kit: the unique identification of the kit; andinformation that associates the unique identification of the kit with the expiration date of the test tube in the kit having the earliest expiration date. 2. A system according to claim 1, further comprising at least one blood collection container having a computer-readable representation of data including the unique identification of the kit disposed within each closed container. 3. A system according to claim 1, further comprising material suitable for preparing a venipuncture site for a needle stick disposed within each closed container. 4. A system according to claim 3, wherein the material comprises an antiseptic wipe and an arm scrubbing device. 5. A system according to claim 1, further comprising material suitable for treating a wound after a needle stick at a venipuncture site disposed within each closed container. 6. A system according to claim 5, wherein the material comprises gauze and a bandage. 7. A system according to claim 1, further comprising a blood donor information sheet disposed within each closed container, the blood donor information sheet having a computer-readable representation of data including the unique identification of the kit. 8. A system according to claim 1, wherein the computer-readable representation of data including the unique identification of the kit comprises an optically computer-readable representation of data. 9. A system according to claim 8, wherein the optically computer-readable representation of data comprises a barcode. 10. A system according to claim 8, wherein the optically computer-readable representation of data comprises a concatenated barcode. 11. A system according to claim 1, wherein the computer-readable representation of data including the unique identification of the kit conforms to the International Society of Blood Transfusion system for identifying, labeling and processing human blood known as ISBT 128. 12. A system according to claim 1, wherein the computer-readable representation of data including the unique identification of the kit comprises an RF-ID tag. 13. A system for facilitating collecting donated blood, the system comprising: a plurality of kits, each kit comprising a closed container having a computer-readable representation of data including a unique identification of the kit, the container having disposed therewithin: at least one sealed test tube, devoid of any blood product, having a computer-readable representation of data including the unique identification of the kit and an expiration date of the test tube;at least one blood collection container having a computer-readable representation of data including the unique identification of the kit and an expiration date of the blood collection container; anda release sheet substrate having a plurality of adhesive labels releasably attached thereto, each of the plurality of adhesive labels having a computer-readable representation of data including the unique identification of the kit; anda computerized database storing, for each kit: the unique identification of the kit; andinformation that associates the unique identification of the kit with the earlier of: the expiration date of the blood collection container having the earliest expiration date; andthe expiration date of the tube in the kit having the earliest expiration date. 14. A system according to claim 13, wherein the at least one blood collection container comprises at least one blood bag. 15. A system according to claim 13, wherein the at least one blood collection container comprises at least one blood collection set. 16. A system according to claim 13, wherein the at least one blood collection container comprises at least one container configured for use with an automated whole blood collector. 17. A system according to claim 13, wherein the at least one blood collection container comprises at least one container configured for use with an apheresis system. 18. A system for facilitating collecting donated blood, the system comprising: a plurality of kits, each kit comprising a closed container having a computer-readable representation of data including a unique identification of the kit, the container having disposed therewithin: at least one sealed test tube, each of the at least one sealed test tube being devoid of any blood product and having a computer-readable representation of data including the unique identification of the kit and an expiration date of the test tube;at least one blood collection container, each of the at least one blood collection container being devoid of any blood product and having a computer-readable representation of data including the unique identification of the kit and an expiration date of the blood collection container;a release sheet substrate having a plurality of adhesive labels releasably attached thereto, each of the plurality of adhesive labels having a computer-readable representation of data including the unique identification of the kit;first material suitable for preparing a venipuncture site for a needle stick disposed within the container; andsecond material suitable for treating a wound after a needle stick at a venipuncture site disposed within the container;wherein: the first material and the second material have respective expiration dates; anda computerized database storing, for each kit: the unique identification of the kit; andthe expiration date of the test tube having the earliest expiration date;the expiration date of the blood collection container having the earliest expiration date;the expiration date of the first material; andthe expiration date of the second material.
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