| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9818c4338719e9d221d47d899fa2d7ea |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B2562-0295
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2021-752
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S435-895 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-54373
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-66
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-155
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-157
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-1495
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-14532
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-14535
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-14546
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-1455
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-150358
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-523
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-681
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N21-78
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-6831
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-6802 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-543
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61B5-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-66
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61B5-145 |
| filingDate |
2006-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9d0e9ccb6d61c24948c89d3a538b001f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c99dd29d4e041098b751a645f7495b7c |
| publicationDate |
2020-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
EP-3629005-A1 |
| titleOfInvention |
Analyte detection device and method with hematocrit correction |
| abstract |
An arrangement (10) for measuring the concentration of an analyte contained in a sample of body fluid includes: an assay pad (40) comprising a chemical reagent capable of producing a detectable signal in the form of a reaction spot (50) formed upon reaction with the analyte; a light source (32); a detector array (20); a processor (84) configured to derive a hematocrit level value from the rate of color change at the reaction spot and to calculate a hematocrit-adjusted analyte concentration using the hematocrit level value; and a memory in communication with the processor. |
| priorityDate |
2005-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |