http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2611891-A1
Outgoing Links
| 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/A61B5-6831 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-14546 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-681 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-1455 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-523 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/G01N21-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-150358 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-1495 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-6802 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/G01N33-54373 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-157 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N31-22 |
| 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 | 2006-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CA-2611891-A1 |
| titleOfInvention | Analyte detection devices and methods with hematocrit/volume correction and feedback control |
| abstract | An arrangement (10) for measuring the concentration of an analyte contained in a sample of body fluid includes: an assay pad (40) comprising at least one 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); and a memory (80) in communication with the processor. The memory (80) includes at least one value indicative of one or more of: (i) the level of hematocrit contained in the sample; (ii) the volume of the sample applied to the assay pad; or (iii) imperfections present in the reaction spot; and further including at least one algorithm for calculating the concentration of the analyte contained in the sample. Alternatively, an arrangement (10) is described for measuring the concentration of an analyte contained in a sample of body fluid, the arrangement including: an assay pad (40) comprising at least one 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); a memory (80) in communication with the processor; and at least one catalyst device constructed and arranged to be responsive to control signals. |
| priorityDate | 2005-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 33.