# US 2014/0155781 A1 · Fluid diversion mechanism for bodily-fluid sampling > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 2014/0155781 A1 - Document ID: US20140155781A1 - Status: Published application - Kind: A1 - Application number: 13/904,691 - Filed: 2013-05-29 - Published: 2014-06-05 - Earliest claimed: 2012-05-30 - Assignees: Magnolia Medical Technologies, Inc. - Applicants: Magnolia Medical Technologies, Inc - Inventors: Gregory J. Bullington; Richard G. Patton; Jay M. Miazga; Shan E. Gaw - Web page: https://patentgrep.com/patent/US20140155781A1 ## CPC - A61B 5/150221: {Valves} - A61B 5/1405: {Devices for taking blood samples (devices for taking samples of other body liquids A61B10/0045)} - A61B 5/150099: {by negative pressure, other than vacuum extraction into a syringe by pulling on the piston rod or into pre-evacuated tubes} - A61B 5/150229: {Pumps for assisting the blood sampling} - A61B 5/150236: {Pistons, i.e. cylindrical bodies that sit inside the syringe barrel, typically with an air tight seal, and slide in the barrel to create a vacuum or to expel blood} - A61B 5/150251: {Collection chamber divided into at least two compartments, e.g. for division of samples (injection syringes having more than one chamber A61M5/19; syringes for injection of two or more media A61M5/2448, A61M5/284; sample preparation for further analysis A61B5/150755)} - A61B 5/150946: {Means for varying, regulating, indicating or limiting the speed or time of blood collection} - A61B 5/150992: {Blood sampling from a fluid line external to a patient, such as a catheter line, combined with an infusion line; Blood sampling from indwelling needle sets, e.g. sealable ports, luer couplings or valves} - A61B 5/153: {Devices} specially adapted for taking samples of venous or arterial blood, e.g. with syringes - A61B 5/15003: {for venous or arterial blood} - A61B: DIAGNOSIS; SURGERY; IDENTIFICATION (usefulness limited to only animals A61D) ## Abstract An apparatus includes a housing, a fluid reservoir, a flow control mechanism, and an actuator. The housing defines an inner volume and has an inlet port that can be fluidically coupled to a patient and an outlet port. The fluid reservoir is disposed in the inner volume to receive and isolate a first volume of a bodily-fluid. The flow control mechanism is rotatable in the housing from a first configuration, in which a first lumen places the inlet port is in fluid communication with the fluid reservoir, and a second configuration, in which a second lumen places the inlet port in fluid communication with the outlet port. The actuator is configured to create a negative pressure in the fluid reservoir and is configured to rotate the flow control mechanism from the first configuration to the second configuration after the first volume of bodily-fluid is received in the fluid reservoir. ## Claims ### Claim 1 A device for procuring bodily-fluid samples from a patient, the device comprising: a housing including a proximal end portion and a distal end portion and defining an inner volume therebetween, the housing having an inlet port configured to be fluidically coupled to the patient, and an outlet port configured to be fluidically coupled to a sample reservoir; a fluid reservoir disposed in the inner volume and configured to receive and isolate a first volume of bodily-fluid withdrawn from the patient; a flow control mechanism disposed in the housing and defining a first lumen and a second lumen, the flow control mechanism configured for rotational movement from a first configuration, in which the inlet port is placed in fluid communication with the fluid reservoir such that bodily-fluid can flow from the inlet port, through the first lumen and to the fluid reservoir, to a second configuration, in which the inlet port is placed in fluid communication with the outlet port such that the bodily-fluid can flow from the inlet, through the second lumen and to the outlet port; and an actuator operably coupled to the flow control mechanism and configured to create a negative pressure in the fluid reservoir when actuated by a user, the actuator further configured to rotate the flow control mechanism from the first configuration to the second configuration after the first volume of bodily-fluid is received in the fluid reservoir from the patient. ### Claim 2 (depends on 1) The device of claim 1, wherein the actuator is further configured to move a first distance to create the negative pressure in the fluid reservoir when actuated by a user. ### Claim 3 (depends on 2) The device of claim 2, wherein the actuator is further configured to move a second distance to rotate the flow control mechanism from the first configuration to the second configuration. ### Claim 4 (depends on 1) The device of claim 1, wherein the actuator is configured to move in a first direction to create the negative pressure in the fluid reservoir, and to move in a second direction to reduce the negative pressure created in the fluid reservoir from movement in the first direction. ### Claim 5 (depends on 1) The device of claim 1, wherein the actuator is configured to allow the user to modulate the negative pressure created in the fluid reservoir. ### Claim 6 A device for procuring bodily-fluid samples from a patient, the device comprising: a housing including a proximal end portion and a distal end portion and defining an inner volume therebetween; an actuator movably disposed in the housing, the actuator including a sealing member and a fluid reservoir defined at least in part by the sealing member, the actuator configured to create a negative pressure in the fluid reservoir when actuated by a user; a diverter disposed in the housing, the diverter having an inlet port configured to be fluidically coupled to the patient, a first outlet port configured to be fluidically coupleable to the fluid reservoir, and a second outlet port configured to be fluidically coupled to a sample reservoir; and a flow control mechanism disposed in the diverter and defining a first lumen and a second lumen, the flow control mechanism configured for rotational movement between a first configuration, in which the inlet port is placed in fluid communication with the first outlet port such that bodily-fluid can flow from the inlet port, through the first lumen and to the first outlet port, to a second configuration, in which the inlet port is placed in fluid communication with the second outlet port such that the bodily-fluid can flow from the inlet, through the second lumen and to the second outlet port. ### Claim 7 (depends on 6) The device of claim 6, wherein the actuator is further configured to rotate the flow control mechanism from the first configuration to the second configuration after a first volume of bodily-fluid is received in the fluid reservoir from the patient. ### Claim 8 (depends on 7) The device of claim 7, wherein the actuator is configured to move a first distance to create the negative pressure in the fluid reservoir, and to move a second distance to rotate the flow control mechanism from the first configuration to the second configuration, when actuated by a user. ### Claim 9 (depends on 6) The device of claim 6, wherein the actuator is configured to move in a first direction to create the negative pressure in the fluid reservoir, and to move in a second direction to reduce the negative pressure created in the fluid reservoir from movement in the first direction. ### Claim 10 (depends on 6) The device of claim 6, wherein the actuator further includes a plunger operably coupled to the sealing member. ### Claim 11 (depends on 10) The device of claim 10, wherein the actuator further includes a spring operably coupled to the plunger, the spring configured to compress in response to an activation force when the actuator is actuated by a user. ### Claim 12 (depends on 11) The device of claim 11, wherein the spring is configured to expand and exert a reaction force when the activation force is removed. ### Claim 13 (depends on 12) The device of claim 12, wherein the spring is configured to allow the user to modulate the negative pressure created in the fluid reservoir. ### Claim 14 A device for procuring bodily-fluid samples from a patient, the device comprising: a housing including a proximal end portion and a distal end portion and defining an inner volume therebetween, the housing having an inlet port configured to be fluidically coupled to the patient, and an outlet port configured to be fluidically coupled to a sample reservoir; a flow control mechanism disposed in the housing and defining a first lumen and a second lumen, the flow control mechanism configured for rotational movement between a first configuration, in which the inlet port is placed in fluid communication with a fluid reservoir defined at least in part by the housing such that bodily-fluid can flow from the inlet port, through the first lumen and to the fluid reservoir, to a second configuration, in which the inlet port is placed in fluid communication with the outlet port such that the bodily-fluid can flow from the inlet, through the second lumen and to the outlet port; and an actuator movably disposed in the housing and operably coupled to the flow control mechanism, the actuator configured to create a negative pressure in the fluid reservoir when actuated by a user, the actuator further configured to rotate the flow control mechanism from the first configuration to the second configuration after a first volume of bodily-fluid is received in the fluid reservoir from the patient. ### Claim 15 (depends on 14) The device of claim 14, wherein the actuator includes an activation mechanism configured to rotate the flow control mechanism from the first configuration to the second configuration. ### Claim 16 (depends on 15) The device of claim 15, wherein the activation mechanism includes a first set of protrusions and the flow control mechanism includes a second set of protrusions, the first set of protrusions configured to operably engage the second set of protrusions to rotate the flow control mechanism from the first configuration to the second configuration. ### Claim 17 (depends on 14) The device of claim 14, wherein the actuator is further configured to create the negative pressure in the fluid reservoir when the actuator is moved from a first position to a second position by the user. ### Claim 18 (depends on 17) The device of claims 17, wherein the actuator is further configured to rotate the flow control mechanism from the first configuration to the second configuration when the actuator is moved from the second position to a third position by the user. ### Claim 19 (depends on 18) The device of claim 18, wherein the actuator includes an activation mechanism and the flow control mechanism includes a set of protrusions, the activation mechanism configured to operably engage the set of protrusions to rotate the flow control mechanism from the first configuration to the second configuration when the actuator is moved from the second position to a third position by the user. ### Claim 20 A device for procuring bodily-fluid samples from a patient, the device comprising: a housing including a proximal end portion and a distal end portion and defining an inner volume therebetween, the housing having an inlet port configured to be fluidically coupled to the patient; a seal member movably disposed in the inner volume; a fluid reservoir disposed in the inner volume and at least partially defined by the seal member, the fluid reservoir configured to receive and isolate a first volume of bodily-fluid withdrawn from the patient; a flow control mechanism movably disposed in the housing, the flow control mechanism configured to move between a first configuration, in which the bodily-fluid can flow from the inlet port, through the flow control mechanism and to the fluid reservoir, and a second configuration, in which the fluid reservoir is fluidically isolated from the inlet port; and an actuator operably coupled to the seal member and to the flow control mechanism, the actuator including a spring configured to move the seal member from a first position to a second position to create a negative pressure in the fluid reservoir, the actuator further configured to move the flow control mechanism from the first configuration to the second configuration after a first volume of bodily-fluid is received in the fluid reservoir from the patient. ### Claim 21 (depends on 20) The device of claim 20, further comprising: a throttling button operably coupled to the actuator and configured to modulate the rate at which the spring moves the seal member from the first position to the second position based on user manipulation of the throttling button. ### Claim 22 (depends on 20) The device of claim 20, wherein the flow control mechanism includes a first control member and a second control member, the second control member defining a first lumen and a second lumen, the flow control mechanism configured for rotational movement between the first configuration in which the inlet port is placed in fluid communication with the fluid reservoir such that bodily-fluid can flow from the inlet port, through the first lumen and to the fluid reservoir, to a second configuration, in which the inlet port is placed in fluid communication with a sample reservoir such that the bodily-fluid can flow from the inlet, through the second lumen and to the sample reservoir. ### Claim 23 (depends on 22) The device of claim 22, wherein the first control member includes a protrusion movably disposed in a grove defined by the second control member, the protrusion configured to move in the grove as the spring moves the seal member from the first position to the second position. ### Claim 24 (depends on 23) The device of claim 23, wherein the protrusion is configured to rotate the second control member when the spring moves the seal member from the second position to a third position. ### Claim 25 A device for procuring bodily-fluid samples from a patient, the device comprising: a housing including a proximal end portion and a distal end portion and defining an inner volume therebetween, the housing having an inlet port configured to be fluidically coupled to the patient, and an outlet port configured to be fluidically coupled to a sample reservoir; a flow control mechanism disposed in the housing, the flow control mechanism including a first control member and a second control member, the second control member defining a first lumen and a second lumen and configured for rotational movement between a first configuration in which the inlet port is placed in fluid communication with a fluid reservoir defined at least in part by the housing such that bodily-fluid can flow from the inlet port, through the first lumen and to the fluid reservoir, to a second configuration, in which the inlet port is placed in fluid communication with the outlet port such that the bodily-fluid can flow from the inlet, through the second lumen and to the outlet port; and an actuator movably disposed in the housing and operably coupled to the first control member, the actuator configured to create a negative pressure in the fluid reservoir when actuated by a user, the actuator further configured to rotate the second control member from the first configuration to the second configuration after a first volume of bodily-fluid is received in the fluid reservoir from the patient. ### Claim 26 (depends on 25) The device of claim 25, wherein the actuator includes an activation mechanism operably coupled to the first control member and configured to rotate the second control member from the first configuration to the second configuration. ### Claim 27 (depends on 25) The device of claim 25, wherein the actuator is further configured to create the negative pressure in the fluid reservoir when the actuator is moved from a first position to a second position by the user. ### Claim 28 (depends on 27) The device of claims 27, wherein the actuator is further configured to rotate the second control member from the first configuration to the second configuration when the actuator is moved from the second position to a third position by the user. ### Claim 29 (depends on 28) The device of claim 28, further comprising: an activation mechanism coupled to the first control member, the activation mechanism including a protrusion configured to operably engage the actuator when the actuator is moved from the second position to a third position by the user.