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US Patent 11660030 Syringe-based fluid diversion mechanism for bodily fluid sampling

Patent 11660030 was granted and assigned to Magnolia Medical Technologies on May, 2023 by the United States Patent and Trademark Office.

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Contents

Is a
Patent
Patent
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Patent attributes

Patent Applicant
Magnolia Medical Technologies
Magnolia Medical Technologies
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Current Assignee
Magnolia Medical Technologies
Magnolia Medical Technologies
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Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
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Patent Number
116600300
Date of Patent
May 30, 2023
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Patent Application Number
177104110
Date Filed
March 31, 2022
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Patent Citations
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US Patent 7351228 Plunger rod for arterial blood collection syringes
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US Patent 7384416 Device and method for irreversible closure of fluid communication in a container system
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US Patent 7461671 Automatic sample collector
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US Patent 7479131 Biological fluid sampling apparatus, assembly and method
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US Patent 7614857 Medical pump device
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US Patent 7615033 Flashback blood collection needle
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US Patent 7648491 Medical substance transfer system
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US Patent 7666166 Bloodless intravenous integrated catheter
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...
Patent Citations Received
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US Patent 11903710 Fluid control devices and methods of using the same
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US Patent 11903709 Fluid control devices and methods of using the same
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US Patent 11963769 Blood sample optimization system and blood contaminant sequestration device and method
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US Patent 11998332 Fluid diversion mechanism for bodily-fluid sampling
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US Patent 12133968 Systems and methods for delivering a fluid to a patient with reduced contamination
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US Patent 11890452 Systems and methods for delivering a fluid to a patient with reduced contamination
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Patent Primary Examiner
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Daniel L Cerioni
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CPC Code
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A61B 5/153
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A61B 5/154
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A61B 5/155
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A61B 5/150732
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A61B 10/0045
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B01L 3/0231
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A61B 5/150251
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A61B 5/1405
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A syringe-based device includes a housing, a pre-sample reservoir, and an actuator. The housing defines an inner volume between a substantially open proximal end portion and a distal end portion that includes a port couplable to a lumen-defining device. The pre-sample reservoir is fluidically couplable to the port to receive and isolate a first volume of bodily fluid. The actuator is at least partially disposed in the inner volume and has a proximal end portion that includes an engagement portion and a distal end portion that includes a sealing member. The engagement portion is configured to allow a user to selectively move the actuator between a first configuration such that bodily fluid can flow from the port to the pre-sample reservoir, and a second configuration such that bodily fluid can flow from the port to a sample reservoir defined at least in part by the sealing member and the housing.

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