The disclosed apparatus, systems and methods relate to devices, systems and methods for the collection of bodily fluids involving a single-use actuation and retraction mechanism disposed within a collector.

The invention relates to a blocking mechanism for a skin incision device and to a method of controlling of a skin incision device by a blocking mechanism. The blocking mechanism comprises a blocking means and a trigger means, which by, respectively, a fixing means and a locating means are mounted in a housing of the cooperating incision device, and which are provided with an engaging means configured to cooperate mutually with each other so that an inadvertent firing of the blocking mechanism and an inadvertent actuation of the incision device prior to use of the device as well as a re-use of the device is not possible, and an indication of a state of use of the device by the blocking means and the trigger means is unambiguous.

The present invention generally relates to receiving bodily fluid through a device opening. In one aspect, the device includes a flow activator arranged to cause fluid to be released from a subject. A deployment actuator may actuate the flow activator in a deployment direction, which may in turn cause fluid release from a subject. The flow activator may also be moved in a retraction direction by a retraction actuator. In one aspect, the device may include a rotatable element that actuates the deployment actuator.

The present disclosure is a blood collection assembly that has a needle assembly fixedly coupled to a finger-activated actuator and tubing and the needle assembly has a needle. Further, the blood collection assembly has a hub that houses the needle assembly and the hub has a channel in a top surface of the hub. Additionally, the channel slidably engages the finger-activated actuator such that when the finger-activated actuator is moved from a distal end of the hub to a proximal end of the hub the needle retracts within the hub.

A body fluid extraction device for extracting a body fluid and for testing a predetermined analyte or property of the fluid comprises a hollow needle having a channel linking a base end and a tip in fluid communication, a collection chamber having an input end in fluid communication with the channel, the collection chamber comprising a capillary wick configured to transport at least a fraction of the body fluid away from the input end, a testing chamber comprising a testing unit that includes a reacting material configured to react to a predetermined analyte or property of the body fluid, a solution chamber, comprising a buffer solution and flow control means configured to control, a first transfer of the buffer solution from the solution chamber to the collection chamber, and a second transfer of the body fluid from the collection chamber to the testing chamber.

A medical needle holder (10) having a generally hollow body (18) which extends in the direction of an axis (62) from a first end (20) to a second end (22). The first end is shaped for reception of a needle (50) therein and the second end is open to allow for insertion of a fluid receptacle (16). The first axis is substantially aligned in use with a needle positioned in the first end of the body. The needle holder comprises a grip portion (28) which extends outwardly from the body in a direction which is angularly offset from the first axis. The grip portion may be actuable between an in-use condition and a disposal condition in which the grip portion covers a needle in the needle holder. The body (18) may comprise control formations on its inner surface to allow for control over the insertion of a fluid receptacle (16) into the body.

A needle guard (10) has an elongate concave channel member (22) having a longitudinally extending opening between two longitudinally extending sides (30) and defining part of a passageway (36) having a forward end (40) and a rear end (64). A tongue member (24), in an open position, extends longitudinally adjacent the opening and defines at least one slot (34) between itself and at least one of the sides (30) adapted to receive at least one wing of a winged needle block. The tongue member (24) is movable to a closed position to lie within the channel member (22) to close, block or substantially close or block the passageway (36).

There is provided an injector having an improvement in a linear launching profile. The injector of the present invention is used for launching a lancet to provide a pricking. The injector of the present invention comprises a plunger capable of launching the lancet in a pricking direction, an injector housing which surrounds the plunger, and an injector cap capable of being attached and detached with respect to the injector housing. In particular, an inner face of the injector cap is provided with a rib, and the rib and the plunger moving for the pricking are capable of contacting with each other.

A lancing device includes a lancet body (14) of elongate form and having a sharp tip (16) at the forward end thereof; a drive spring (26) for imparting generally longitudinal movement to the lancet body, and a housing (10) receiving the lancet body and having an aperture (22) in the forward end thereof through which the sharp tip (16) of the lancet body projects in use when the device is fired. The device includes elements (28, 30, 32) for controlling movement of the lancet body (14) to cause the tip of the lancet to execute a lateral movement when it projects from the aperture.

The present disclosure provides a device for collecting a bodily fluid sample of a subject for nucleic acid amplification, a method for collecting a bodily fluid sample of a subject for nucleic acid amplification, and a kit for nucleic acid amplification. The device may comprise a device body that is coupled to at least one collection channel including a collection member having an opening at an end thereof to permit flow of the bodily fluid sample from a source thereof to the collection channel. The collection channel may be substantially free of an anticoagulant. The device may further comprise a mechanical member coupled to the device body. The mechanical member may actuate the collection member to (i) extend away from the collection channel for collection of the bodily fluid sample from the source thereof, and (ii) retract into the collection channel upon collection of the sample.