Bodily fluid sample collection systems, devices, and method are provided. The device may comprise a first portion comprising at least a sample collection channel configured to draw the fluid sample into the sample collection channel via a first type of motive force. The sample collection device may include a second portion comprising a sample container for receiving the bodily fluid sample collected in the sample collection channel, the sample container operably engagable to be in fluid communication with the collection channel, whereupon when fluid communication is established, the container provides a second motive force different from the first motive force to move a majority of the bodily fluid sample from the channel into the container.

A lancet pricking device comprises a lancet, a launching spring, a trigger part and a holder housing the lancet, launching spring and trigger part. The lancet comprises a lancet body, lancet cap and pricking needle. The pricking needle is in both the lancet body and lancet cap. The trigger part has a pair of arms positioned inside the holder. The launching spring is attached to the lancet body. The lancet body is secured to the arms of the trigger part by an abutment of the lancet body on the arms such that the launching spring is compressed before a pricking operation. The trigger part cannot be pushed toward the inside of the holder before the lancet cap is removed, but can be pushed toward the inside of the holder after the cap is removed. The lancet body warps when pressed to release the secured lancet body.

A lancing actuator (114) includes a drive element (118) for driving a lancing element, the drive element being guided within a housing (112), a combined compression and torsion element (120) which, by a relaxing movement thereof, is adapted to drive the lancing motion, a combined triggering and driving device (122) having an actuating element (124) and a locking device (126), wherein the actuating element has an initial state and an actuated state and is accessible from the outside of the housing, wherein, in the initial state, the drive element is locked in the locking device under a torsional stress exerted by the combined compression and torsion element, wherein the combined triggering and driving device is configured in a manner that, when the actuating element makes a movement along an actuation path from the initial state into the actuated state, a torque is exerted on the drive element which prevails over the torsional stress exerted by the combined compression and torsion element such that the drive element is released from the locking device, which results in a triggering of the lancing motion.

A puncture needle cartridge (1) includes: a lancet body (5) mounted with a puncture needle (3) on a front end side and having a mount (4) on a rear end side; and a plate-like first case (6) and second case (7) covering the lancet body (5) from above and below and arranged slidably back and forth along each other. The puncture needle cartridge (1) is configured such that the first case (6) is slid forward of the second case (7), and in this slid state, the first case (6) and the second case (7) are secured to each other when ejected from the puncture instrument (10). This can make the puncture needle cartridge (1) impossible to mount again on the puncture instrument (10).

The medical puncturing device includes a housing, a shield, and a skin puncturing assembly disposed within the housing. The shield is axially movable in the housing. The skin puncturing assembly includes a movable carrier and a skin puncturing element mounted to the carrier. A distal end of the skin puncturing element is adapted for puncturing the skin of a patient. The carrier is movable from a retracted position wherein the skin puncturing element is disposed within the shield to a puncturing position wherein the distal end of the skin puncturing element is exposed. The carrier is maintained in the retracted position by engagement of flexure members or a retaining tab with the carrier. A drive spring is provided to move the carrier from the retracted position to the puncturing position. A retraction spring is provided to return the carrier and skin puncturing element into the housing.

Bodily fluid sample collection systems, devices, and method are provided. The sample is collected at a first location and subjected to a first sample processing step. The sample may be shipped to a second location and subjected to a second sample processing step that does not introduce contaminants into a plasma portion of the sample formed from the first processing step. The sample may also be mixed with other material(s) in the collection device.

Bodily fluid sample collection systems, devices, and method are provided. The device may comprise a first portion comprising at least a sample collection channel configured to draw the fluid sample into the sample collection channel via a first type of motive force. The sample collection device may include a second portion comprising a sample container for receiving the bodily fluid sample collected in the sample collection channel, the sample container operably engagable to be in fluid communication with the collection channel, whereupon when fluid communication is established, the container provides a second motive force different from the first motive force to move a majority of the bodily fluid sample from the channel into the container.

A disposable automatic painless safe hemostix includes an outer casing, an inner sleeve, a needle module and a spring. The needle module is snapped in the inner sleeve and the outer casing. The needle module has a needle point protecting pole. Interlock fixing faces and protrusions are provided on the inner sleeve. Interlock guiding slopes and protrusion stoppers are provided on the inner wall of the outer casing. One end of the interlock engages the interlock fixing face, and the other end engages the interlock guiding slope.

Bodily fluid sample collection systems, devices, and method are provided. The device may comprise a first portion comprising at least a sample collection channel configured to draw the fluid sample into the sample collection channel via a first type of motive force. The sample collection device may include a second portion comprising a sample container for receiving the bodily fluid sample collected in the sample collection channel, the sample container operably engagable to be in fluid communication with the collection channel, whereupon when fluid communication is established, the container provides a second motive force different from the first motive force to move a majority of the bodily fluid sample from the channel into the container.

An integrated testing device and method are disclosed. The device includes an integral reservoir for a test fluid, and an actuator, so that the test fluid can be dispensed to facilitate the test.