US2023172502A1PendingUtilityA1

Fluid diversion mechanism for bodily-fluid sampling

Assignee: MAGNOLIA MEDICAL TECHNOLOGIES INCPriority: May 30, 2012Filed: Jul 13, 2022Published: Jun 8, 2023
Est. expiryMay 30, 2032(~5.8 yrs left)· nominal 20-yr term from priority
A61B 5/150992A61B 5/153A61B 5/150389A61B 5/155A61B 5/150236A61B 10/0048A61B 2010/0061A61B 2010/008A61B 5/150503A61B 5/150244A61B 5/150251A61B 5/15003A61B 10/0051A61B 5/150221A61B 2010/0077A61B 10/007
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Claims

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

exact text as granted — not AI-modified
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  a fluid reservoir disposed in the inner volume and configured to receive and isolate a first volume of bodily-fluid withdrawn from the patient;   a flow control mechanism disposed in the housing and defining a first lumen and a second lumen, the flow control mechanism configured for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.   
     
     
         2 . 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. 
     
     
         3 . 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. 
     
     
         4 . 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. 
     
     
         5 . The device of  claim 1 , wherein the actuator is configured to allow the user to modulate the negative pressure created in the fluid reservoir. 
     
     
         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.   
     
     
         7 . 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. 
     
     
         8 . 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. 
     
     
         9 . 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. 
     
     
         10 . The device of  claim 6 , wherein the actuator further includes a plunger operably coupled to the sealing member. 
     
     
         11 . 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. 
     
     
         12 . The device of  claim 11 , wherein the spring is configured to expand and exert a reaction force when the activation force is removed. 
     
     
         13 . The device of  claim 12 , wherein the spring is configured to allow the user to modulate the negative pressure created in the fluid reservoir. 
     
     
         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.   
     
     
         15 . 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. 
     
     
         16 . 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. 
     
     
         17 . 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. 
     
     
         18 . 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. 
     
     
         19 . 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. 
     
     
         20 - 39 . (canceled)

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