Patent classifications
A61B5/15111
Body fluid sampling arrangements
An arrangement for producing a sample of body fluid from an opening created in a skin surface at a sampling site including a cartridge with a plurality of compartments and a plurality of sampling sites, and a detector assembly. Each sampling site includes a skin-penetration member having a first end configured to pierce the surface of the skin and an inner lumen in communication with the first end, a spring actuator operatively associated with the skin-penetration member, and a needle hub connecting the skin-penetration member and the spring actuator. The needle hub includes a reagent pad and the spring actuator is configured to drive the skin-penetration member to form the wound opening. Each compartment at least partially encloses the skin-penetration member, the spring actuator, and the needle hub of a respective sampling site.
Devices and methods for body fluid sampling and analysis
Described here are meters and methods for sampling, transporting, and/or analyzing a fluid sample. The meters may include a meter housing and a cartridge. In some instances, the meter may include a tower which may engage one or more portions of a cartridge. The meter housing may include an imaging system, which may or may not be included in the tower. The cartridge may include one or more sampling arrangements, which may be configured to collect a fluid sample from a sampling site. A sampling arrangement may include a skin-penetration member, a hub, and a quantification member.
Blood sampling devices
A blood sampling device includes a housing and a lancet supporting a lancet needle or tip, the lancet and needle being urged or urgeable in a pricking direction. A trigger mechanism is moveable to a fire position for releasing the lancet to travel in the pricking direction. A removable safety cap initially covers the lancet needle. The lancet has an initial position in which movement of the trigger mechanism to the fire position is blocked and an intermediate position in which the trigger mechanism may be moved to the fire position. The intermediate position is obtainable only on removal of the safety cap.
Devices and methods for body fluid sampling and analysis
Described here are meters and methods for sampling, transporting, and/or analyzing a fluid sample. The meters may include a meter housing and a cartridge. In some instances, the meter may include a tower which may engage one or more portions of a cartridge. The meter housing may include an imaging system, which may or may not be included in the tower. The cartridge may include one or more sampling arrangements, which may be configured to collect a fluid sample from a sampling site. A sampling arrangement may include a skin-penetration member, a hub, and a quantification member.
Single-handed operable infant heel blood sampling device and its safety mechanism
The disclosure discloses a single-handed operable infant heel blood sampling device and its safety mechanism, including a push-pull rod and an actuating rod partially extending outside the blood sampler housing; the actuating rod has a second hook portion that can engage with the first hook portion; to perform blood sampling, push down the push-pull rod to disengage the buckle portion from the housing, causing the first hook portion to engage with the second hook portion on the first end of the actuating rod; then pull up the push-pull rod to pull the actuating rod, and the actuating rod thus releases a pre-compressed spring set inside the blood sampler housing, allowing the blade originally positioned in a first position inside the housing to slide out from a cutting port and then be retracted into a second position inside the housing.
MINIATURE SAFETY BLOOD LANCET FOR MINIMIZING PAIN
A miniature safety blood lancet for minimizing pain includes a needle body, an activation sleeve, a housing and a spring. The activation sleeve is arranged in the housing. The needle body is arranged in the activation sleeve. The housing, the activation sleeve and the needle body are slidably connected. The activation sleeve is provided with an inner wall. The inner side of the middle of the inner wall is provided with an unlocking arm, and the outer side of the bottom of the inner wall is provided with a buckle. A needle cap is arranged at the front end of the needle body. The unlocking arm of the activation sleeve is snap-fitted with a self-locking protrusion of the needle cap and an inverted buckle of the housing, respectively. The spring is arranged between the bottom of the needle body and the housing.
Bodily fluid sample collection and transport
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.
Lancing device with rear adjustment of penetration depth
A lancing device with rear adjustment of penetration depth includes a cap, cap holder, ejection pin and shell, wherein: the lancing device has an external and medium depth adjusting sleeve. The ejection pin is located in the medium sleeve and the external depth adjusting sleeve is sleeved outside the medium sleeve; the external sleeve connects axially and circumferentially to the shell, and a rotary locating mechanism is between the external sleeve and the shell; the medium sleeve is connected circumferentially and axially in a sliding way, and a rotary moving mechanism is between the medium the external sleeve, and the medium includes a passive impact face relative to the active impact face of the ejection pin; the external sleeve includes a manual adjusting ring outside the lancing device at the middle and rear part, and rotates to drive the medium sleeve to move axially, changing the needle tip penetration depth.
INSERTING DEVICE AND BLOOD COLLECTION DEVICE
An inserting device includes a main casing, a bracket, a first elastic component, an inserting assembly and a second elastic component. The main casing has a position-limiting portion and a first holding portion. The bracket is disposed in the main casing and has a second holding portion. The first elastic component is disposed between the main casing and the bracket, and the first holding portion holds the bracket. The inserting assembly is disposed in the main casing. The second elastic component is disposed between the inserting assembly and the bracket. The position-limiting portion limits the second holding portion, such that the second holding portion holds the inserting assembly on the bracket. When the bracket is released by the first holding portion, the bracket, the second elastic component and the inserting assembly move by the elastic force of the first elastic component, the second holding portion is departed from the position-limiting portion, and the inserting assembly is restored by an elastic force of the second elastic component. Moreover, a blood collection device including the inserting device is also provided.
Lancing device having anesthetic feature
A handheld lancing device having anesthetic feature includes a housing removably retaining a disposable lancet. A carriage suspended within the housing by an isolation assembly may receive the lancet. A motor in mechanical communication with the lancet produces vibrations transmitted to contact surface, which vibrate a target lancing site prior to and during piercing. The target site is vibrated for a predetermined period of time before deploying the lancet. The isolation assembly permits movement of the carriage and/or lancet within the housing in one direction while limiting movement in other directions, and further dampens the vibrations of the motor from the housing held by the user. A force sensor detects force applied by the pressing of the contact surface against the skin of the patient. An indicator(s) perceivable to the user identifies when predefined positions of the lancet are reached for initiating vibration then triggering the lancet.