http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2554338-T3
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9605966a4bfd111f3166a10b18539524 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B6-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B6-481 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-0046 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-14546 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B6-504 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B8-481 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-055 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-201 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61B5-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61B5-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61B6-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61B8-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61B5-145 |
filingDate | 2005-10-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2015-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6f1082696de75bb74c15181d4733f529 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_054b524540aa9ce55b956eb167b4dc4b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f8a180b41437f901fe083a4c78f28b60 |
publicationDate | 2015-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | ES-2554338-T3 |
titleOfInvention | Medical imaging system, dispensing system, method, and software product to evaluate the patient's renal function before administering a contrast medium as part of a medical imaging procedure |
abstract | A dispensing system adapted to administer a contrast medium used in a medical imaging procedure, the dispensing system comprising: a dispensing device (120) configured to deliver the contrast medium to a patient; an analysis device (130) adapted to receive and analyze a biological fluid sample from the patient to determine a level of at least one substance in the biological fluid sample, the analysis device (130) being adapted to inform an operator of the system of the level of the at least one substance, the analysis device (130) being further adapted to inform the operator whether the level of the at least one substance is within a selected range, and the analysis device (130) being further adapted to be in communication with the dispensing device (120) as to whether to administer the contrast medium; wherein the at least one substance is selected from the group consisting of: blood urea nitrogen (BUN); creatinine; or combinations thereof. |
priorityDate | 2004-10-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 30.