摘要:
Drug delivery safety devices comprise a safety needle device comprising a needle hub, a needle cannula, and a safety feature; and a cap comprising a cap body having a proximal end attached to the safety needle device and a distal end having an access opening that is in fluid communication with the needle cannula. The safety needle device allow for an integrated device for both filling and injection that do not interfere with passive safety features. The caps may have a fill feature that engages with a safety feature of the safety needle device to keep it in a fill state.
摘要:
Drug delivery safety devices comprise a safety needle device comprising a needle hub, a needle cannula, and a safety feature; and a cap comprising a cap body having a proximal end attached to the safety needle device and a distal end having an access opening that is in fluid communication with the needle cannula. The safety needle device allow for an integrated device for both filling and injection that do not interfere with passive safety features. The caps may have a fill feature that engages with a safety feature of the safety needle device to keep it in a fill state.
摘要:
Detection systems for a syringe assembly that provide precision in monitoring the amount of fluid contained within the syringe barrel, detecting motion of the plunger within the syringe barrel, detecting the position of the plunger within the syringe barrel, and/or monitoring the volume received within or delivered by the syringe assembly are disclosed. A detection system of the present disclosure allows a sensor in communication with a portion of a plunger assembly to sense the motion of a plunger rod relative to a syringe barrel and thereby volume received within or delivered by the syringe by reading gradations having an identifier directly as the plunger rod with sensor moves past each respective gradation with identifier.
摘要:
Provided is a method for vascular access device placement. The method may include receiving clinician data associated with at least one clinician including a first clinician. Patient data associated with at least one patient including a first patient may be received. At least one first probability of successful placement of at least one vascular access device by the first clinician at at least one access point of the first patient may be generated based on the patient data associated with the first patient and the clinician data associated with the first clinician. An instruction message for placement of the at least one vascular access device may be communicated based on the at least one first probability to a user device. A system and computer program product are also disclosed.
摘要:
A method may include obtaining, with a first temperature sensor, a first temperature measurement at a first location on a body of a patient adjacent a catheter insertion site of a catheter; obtaining, with an array of temperature sensors, a plurality of temperature measurements at a plurality of locations on the body of the patient, each of the plurality of locations being spaced apart from the first location, and the plurality of locations including locations at a plurality of different distances from the first location; determining, with at least one processor, based on the first temperature measurement and the plurality of temperature measurements, an alert condition associated with a dressing and/or securement device and/or the catheter; and in response to determining the alert condition, generating, with at least one processor, an alert to a user.
摘要:
A blood separation and testing system for a blood sample is disclosed. The blood separation and testing system includes a blood sampling transfer device adapted to receive a blood sample, a blood separation device, and a blood testing device. The blood separation device is adapted to receive a portion of the blood sampling transfer device such that with the blood sampling transfer device received within the blood separation device and a rotational force applied to the blood sampling transfer device, a plasma portion of the blood sample is separated from a cellular portion of the blood sample. The blood testing device is adapted to receive a portion of the blood sampling transfer device to analyze the plasma portion of the blood sample and obtain test results.
摘要:
A biological fluid collection device that is adapted to receive a blood sample having a cellular portion and a plasma portion is disclosed. After collecting the blood sample, the biological fluid collection device is able to transfer the blood sample to a point-of-care testing device or a biological fluid separation and testing device. After transferring the blood sample, the biological fluid separation and testing device is able to separate the plasma portion from the cellular portion and analyze the blood sample and obtain test results.
摘要:
A blood separation and testing system for a blood sample is disclosed. The blood separation and testing system includes a blood sampling transfer device adapted to receive a blood sample, a blood separation device, and a blood testing device. The blood separation device is adapted to receive a portion of the blood sampling transfer device such that with the blood sampling transfer device received within the blood separation device and a rotational force applied to the blood sampling transfer device, a plasma portion of the blood sample is separated from a cellular portion of the blood sample. The blood testing device is adapted to receive a portion of the blood sampling transfer device to analyze the plasma portion of the blood sample and obtain test results.
摘要:
A system may include an intravenous (IV) catheter comprising a first portion configured to be inserted into a vein of a patient and a second portion configured to remain outside a patient when the first portion is inserted into the patient. The IV catheter may include a pressure sensor configured to detect a pressure of a fluid associated with the IV catheter. A method may include receiving data associated with the pressure of the fluid associated with the IV catheter, and determining whether the IV catheter is inserted into the vein of the patient based on the pressure of the fluid associated with the IV catheter.
摘要:
A medical waste tracking device may include a housing including an opening configured to receive a medical device and a package for the medical device and/or a sensor configured to determine first identifying information from the package for the medical device and second identifying information from the medical device. One or more processors may be programmed and/or configured to determine, based on the first identifying information, that the medical device is in use; and determine, based on the second identifying information, that the medical device is not in use.