Patent classifications
A61M2210/1007
Breast flange for direct coupling to breast pump fitting
A breast flange has a cup portion shaped to receive a lactating female breast, a funnel portion coupled to the cup portion and shaped to receive areola and nipple regions of the lactating female breast and to be in contact with the areola region, and a neck portion coupled to the funnel portion and configured to be coupled directly to a breast pump fitting. At least the funnel portion is made of a pliable and resilient material, the material having a thickness. The funnel portion has a set of windows, each window defined by a reduction in thickness of the material and configured to deflect in the presence of suction so as to mimic action of a tongue of a nursing baby.
COMPOSITIONS, DEVICES AND KITS FOR SELECTIVE INTERNAL RADIATION THERAPY
Systems, kits and methods for preparing an injection system and/or treating target lesions with a selective internal radiation therapy which includes a double-barrel syringe loaded with a two-component tissue glue and radioisotope loaded microspheres. The microspheres are loaded into the syringe based on the size of the target location and are administered with a needle or dual-lumen catheter. Dosing regimens for treating breast cancer lesions or surgical beds up to 130 mm in diameter and hepatocellular carcinoma lesions up to 50 mm are included.
Suction device for medical use in removing material from a surgical site or similar
A device for evacuating a surgical site of a patient includes a container that defines a first end having a tapered surgical site engaging surface and a second end having a pressure source engaging surface. The first end defines a tapered cross-section configured for being engageably received within an opening at the surgical site. In operation, vacuum pressure is applied to the second end in order to create a vacuum within the container to evacuate fluids from the surgical site.
Breastmilk collection system
A breastmilk collection device includes breast contacting flange, a vacuum reservoir, flexible diaphragm separating the breast contacting flange and the vacuum reservoir, and a flange receiver between the breast contacting flange and the flexible diaphragm. The breast contacting flange has a wide portion for accepting the breast and a narrow portion. The flexible diaphragm is located between the narrow portion and the vacuum reservoir. The flexible diaphragm moves between a sealed configuration, in which the breast contacting flange is sealed off from the vacuum reservoir, and an open valve configuration, in which the flexible diaphragm acts as a one-way valve to allow expressed milk to flow through a milk flow opening between the flexible diaphragm and the breast contacting flange when an opening pressure is reached in the breast contacting flange.
Breastmilk collection system
A breastmilk collection device includes breast contacting flange, a vacuum reservoir, flexible diaphragm separating the breast contacting flange and the vacuum reservoir, and a flange receiver between the breast contacting flange and the flexible diaphragm. The breast contacting flange has a wide portion for accepting the breast and a narrow portion. The flexible diaphragm is located between the narrow portion and the vacuum reservoir. The flexible diaphragm moves between a sealed configuration, in which the breast contacting flange is sealed off from the vacuum reservoir, and an open valve configuration, in which the flexible diaphragm acts as a one-way valve to allow expressed milk to flow through a milk flow opening between the flexible diaphragm and the breast contacting flange when an opening pressure is reached in the breast contacting flange.
Compositions, devices and kits for selective internal radiation therapy
Systems, kits and methods for preparing an injection system and/or treating target lesions with a selective internal radiation therapy which includes a double-barrel syringe loaded with a two-component tissue glue and radioisotope loaded microspheres. The microspheres are loaded into the syringe based on the size of the target location and are administered with a needle or dual-lumen catheter. Dosing regimens for treating breast cancer lesions or surgical beds up to 130 mm in diameter and hepatocellular carcinoma lesions up to 50 mm are included.
FILTER CARTRIDGE ASSEMBLIES FOR MANAGING FLUID AND HUMIDITY IN ENDOSCOPIC SURGERY
A filter cartridge for surgical gas delivery systems includes a filter housing configured to be seated in a filter cartridge interface of a surgical gas delivery system, with a plurality of flow paths defined through the filter housing including at least one evacuation/return flow path and at least one insufflation/sensing flow path. A humidity filter element is included in the evacuation/return flow path for removing humidity from an evacuation/return lumen of a tube set. The humidity filter element can include a sintered polymer material configured to provide tortuous flow paths therethrough to condense humidity out of a flow through the humidity filter element.
Systems, devices and methods for assessing milk volume expressed from a breast
Systems and methods for assessing milk volume changes within a breast are described. Also described are systems and methods for assessing volume changes in the stomach of an infant.
VIBRATORY WAVEFORM FOR BREAST PUMP
A method for facilitating milk extraction from a female breast may involve applying a breast contacting portion of a breast pump system to a breast, activating the breast pump system to administer multiple breast pumping cycles, and applying vibrations to the breast during at least a portion of each of the breast pumping cycles, using a vibration device. A vibration generating device may be a component of a breast pump system, an added attachment on a breast pump system or a separate component that works in conjunction with a breast pump system.
Vibratory waveform for breast pump
A method for facilitating milk extraction from a female breast may involve applying a breast contacting portion of a breast pump system to a breast, activating the breast pump system to administer multiple breast pumping cycles, and applying vibrations to the breast during at least a portion of each of the breast pumping cycles, using a vibration device. A vibration generating device may be a component of a breast pump system, an added attachment on a breast pump system or a separate component that works in conjunction with a breast pump system.