Patent classifications
A61B5/15074
Manual Flow Regulation for Blood Collection
A specimen collection assembly including a flow control member for adjustably altering a flow path is disclosed. In one configuration, the flow control member defines a regulation channel in fluid communication with a lumen of a cannula, wherein the flow control member is configured to adjustably alter an effective flow distance between the lumen of the cannula and an interior of an evacuated collection container. In another configuration, the flow control member is positioned to vary an effective cross-sectional area of at least one of an inlet port and an outlet port adapted to be in fluid communication with the lumen and the evacuated collection container.
DEVICE FOR TRAPPING AN INITIAL FLOW OF BLOOD
Various embodiments of the present disclosure describe a diversion device that traps an initial flow of blood in a diversion chamber of the diversion device. The diversion chamber may be defined, in part, by a housing shell, a housing base, and a filter. The filter may be a porous material that allows air, but not blood, to flow through it. After the diversion chamber is filled, a subsequent flow of blood may be directed into a collection vessel through an internal conduit of the diversion device.
Biological Fluid Separation Device
A biological fluid separation device and a separation process that allows for efficient separation of plasma from a blood sample is disclosed. A biological fluid separation device of the present disclosure is adapted to receive a blood sample having a cellular portion or cells and a plasma portion or plasma. A biological fluid separation device of the present disclosure separates plasma from cells using a track-etched membrane and cross-flow filtration.
Medical device for the preparation of a concentrate of cells
A medical device for the separation of a concentrate enriched with cells from a biological fluid, in particular a concentrate of stromal or stem cells from medullar aspirate or venous blood, comprises: a treatment container for receiving and treating the biological fluid for the purposes of its separation into a number of fractions; a first collection container, for receiving a first fraction of the fluid, in particular a fraction poor in said cells; a second collection container, for receiving a second concentrated fraction of the fluid enriched with said cells; a deviator valve having a first way connected or prearranged for connection to the treatment container, a second way connected or prearranged for connection to the first collection container, and a third way connected or prearranged for connection to the second collection container; a first line for connection of the treatment container to the first way of the deviator valve, a second line for connection of the first collection container to the second way of the deviator valve, and a third line for connection of the second collection container with the third way of the deviator valve. The treatment container is a syringe container with a plunger having a plunger stem associated in a releasable way to a corresponding plunger head, and the first connection line comprises a first transparent tube, in particular a flexible transparent tube, and at least one of the second and third connection lines preferably comprises a second flexible tube. At least one connection line, or each connection line, further comprises: at least one respective hydraulic connector, for separable connection of a corresponding tube to the corresponding container and/or to the corresponding way of the deviator valve; and at least one automatic-closing or one-way valve.
Manual flow regulation for blood collection
A specimen collection assembly (100) including a flow control member (106) for adjustably altering a flow path is disclosed. In one configuration, the flow control member (106) defines a regulation channel (166) in fluid communication with a lumen of a cannula (112), wherein the flow control member (106) is configured to adjustably alter an effective flow distance between the lumen of the cannula (112) and an interior of an evacuated collection container. In another configuration, the flow control member (106) is positioned to vary an effective cross-sectional area of at least one of an inlet port (346) and an outlet port (350) adapted to be in fluid communication with the lumen and the evacuated collection container.
Bodily fluid collection device with integral tube seal
A medical device useful for collecting samples of a bodily fluid, typically a vascular fluid such as blood. The subject device can also be used for infusing liquids into a patient. The fluid flow path desirably includes a forwardly projecting, rearwardly biased needle, a needle holder and a length of plastic tubing, the forwardly extending end of which is configured to function as a fluid seal to reduce the likelihood of fluid leakage during or after use. Following use, the needle is retractable from the patient by sliding a needle retraction cavity transversely into longitudinal alignment with the needle, thereby disrupting the fluid flow path and propelling the needle rearwardly so that it no longer projects from the device.
AUTO-RETRACTABLE SAFETY BLOOD COLLECTION NEEDLE
An auto-retractable blood collection needle, including: a needle holder including a first tube, a second tube and a holder tail; a needle in stalled in the first tube; a built-in sliding sleeve which is elongated and through and has a C-shaped cross section; a needle shield which is hollow and elongated; and a spring sheathed on the first tube. The second tube is installed in the built-in sliding sleeve and is capable of sliding back and forth. The built-in sliding sleeve is installed in the needle shield and is capable of sliding back and forth. A locking mechanism is formed by the holder tail and the needle shield. When the holder tail is unlocked from the needle shield, a force of the spring pushes the second tube to slide backward, and then the built-in sliding sleeve is driven to slide rearward to lock with the needle shield.
Passive Double Drive Member Activated Safety Blood Collection Device
A shieldable needle device including a drive member is disclosed. The drive member is extendable between a biased position and an extended position for moving a tip guard from an first position to a second position in which the tip guard shields a distal end of the needle cannula. The shieldable needle device includes a pair of wings extending laterally from opposing sides of the hub that are movable between a laterally extending position and a dorsal position. With the wings in the dorsal position, the wings retain the drive member in the biased position thereby maintaining the tip guard in the first position. Movement of the wings from the dorsal position to the laterally extending position releases retainment of the drive member. A second drive member may be included.
BLOOD COLLECTION INSTRUMENT AND BLOOD COLLECTION PLATE
A novel blood collection instrument with which it is possible to prevent blood from coming into contact with air during collection of blood, and a blood collection plate that is suitably used therefor. A blood collection instrument including: a blood holding member having a structure in which a plurality of plate-shaped members, are overlapped with each other and including a collected blood holding passage formed between overlapped surfaces of the plate-shaped members; a connection part provided at an inflow port of the collected blood holding passage in the blood holding member; and a puncture member including a puncturing hollow needle while being connected to the connection part. An inner hole of the hollow needle of the puncture member is allowed to communicate with the collected blood holding passage in the blood holding member.
Passively shielding needle assembly with skin sensor
A shielding needle assembly is provided with a hub having a needle cannula with a puncture tip extending from a forward end thereof, and a shield member in telescoping association with the hub. A drive member biases the hub and the shield member away from each other for relative telescopic movement between a first position in which the puncture tip extends from a forward end of the shield member, and a second position in which the puncture tip is encompassed within the shield member. A pivoting lever maintains the hub and the shield member in the first position against the bias of the drive member. The lever is pivotable during contact with a patient's skin surface, thereby releasing the hub and the shield member from the first position and permitting the drive member to bias the hub and the shield member toward the second position.