Abstract: A system and method for imaging a target in a patient's body includes the steps of providing a pre-acquired image of the target and placing a catheter having a position sensor, an ultrasonic imaging sensor and at least one electrode, in the patient's body. Positional information of a portion of the catheter in the patient's body is determined using the position sensor and electrical activity data-points of a surface of the target are acquired using the at least one electrode. An ultrasonic image of the target is obtained using the ultrasonic imaging sensor and positional information for the electrical activity data-points of the surface of the target is determined. An electrophysiological map of the target is generated based on the electrical activity data-points and the positional information for the electrical activity data-points.

Abstract: A method and system for analyzing sounds originating in at least a portion of an individual's cardiovascular system. N transducers, where N is an integer, are fixed on a surface of the individual over the thorax. The ith transducer is fixed at a location xi and generates an initial signal P(xi,i) indicative of pressure waves at the location xi, for i=1 to N. the signals P(xi,t) are processed so as to generate filtered signals in which at least one component of the signals P(xi,t)not arising from cardiovascular sounds has been removed. The filtered signals may be used for generating an image of the at least portion of the cardiovascular system.

Abstract: The invention relates to systems and methods for site selection and placement of extra-anatomic passages altering gaseous flow in a diseased lung.

Abstract: A method for extracting a tissue sample includes altering the pressure inside the lumen of a cannula to facilitate extraction of a tissue sample from the cannula. One aspect of the invention includes a biopsy apparatus comprising a valve for controlling the pressure inside the lumen of the cannula. In one variation, the pressure/vacuum generating device is connected to a cannula with a closed distal end and an orifice located on a circumferential surface of said cannula. A cutting sheath is slidably disposed over said cannula. The valve may be provided between the pressure/vacuum generating device and the cannula to control the pressure within the lumen of the cannula.

Abstract: A biopsy device and method are provided for obtaining a tissue sample, such as a breast tissue biopsy sample. The biopsy device may include an outer cannula having a distal piercing tip, a cutter lumen, a side tissue port communicating with the cutter lumen, and at least one fluid passageway disposed distally of the side tissue port. The inner cutter may be advanced in the cutter lumen past the side tissue port to sever a tissue sample. After the tissue sample is severed, and before the inner cutter is retracted proximally of the side tissue port, the cutter may be used to alternately cover and uncover the fluid passageway disposed distally of the side tissue.

Abstract: A mucous gathering device, comprising an elongated rotatable stem having a longitudinal axis, and a rotary headpiece carried at an end of the stem for angular flexing as the stem rotates, the headpiece having a face sized for presentation to the cervix entrance as the head rotates about an axis angled relative to the stem, the face having associated flexible means for gathering and retaining mucous proximate the cervix as the headpiece rotates, and a flexible rotary probe carried by the headpiece, the probe projecting forwardly and centrally relative to associated means and defining edges spaced apart to gather and propel mucous toward the headpiece in response to probe rotation in an opening defined by the cervix.

Abstract: A therapeutic ball comprises an outer surface having a plurality of projections thereon, and an inner portion comprising a material selected for its ability to retain heat.

Abstract: A system applies cardiopulmonary resuscitation (CPR) to a recipient. An automated controller is provided together with a compression device which periodically applies a force to a recipient's thorax under control of the automated controller. A band is adapted to be placed around a portion of the torso of the recipient corresponding to the recipient's thorax. A driver mechanism shortens and lengthens the circumference of the band. By shortening the circumference of the band, radial forces are created acting on at least lateral and anterior portions of the thorax. A translating mechanism may be a bladder provided for translating the radial forces to increase the concentration of anterior radial forces acting on the anterior portion of the thorax. The driver mechanism may comprise a tension device for applying a circumference tensile force to the band.

Abstract: A resuscitation device for automatic compression of victim's chest using a compression belt which exerts force evenly over the entire thoracic cavity. The belt is constricted and relaxed through a motorized spool assembly which repeatedly tightens the belt and relaxes the belt to provide repeated and rapid chest compression. An assembly includes various resuscitation devices including chest compression devices, defibrillation devices, and airway management devices, along with communications devices and senses with initiate communications with emergency medical personnel automatically upon use of the device.

Abstract: A massaging system includes an input device including a pressure-position profile sensor and a massaging device connected to and responsive to a signal received from the input device, the massaging device configured to massage at least a portion of a human body. A method of massaging includes providing a massaging system, sensing a pressure-position input profile of a manual input to the input device; and applying a pressure-position massage profile to the portion based at least in part on the pressure-position input profile.

Abstract: An emergency system for treatment of a patient (20) experiencing an acute vascular obstruction, employing a non-invasive vibrator (10), optimally in conjunction with drugs, for disrupting and lysing thromboses, relieving spasm (if associated), and thereby restoring blood perfusion. Vibrator (10) is operable in the sonic to infrasonic range, with a source output of up to 15 mm. For acute myocardial infarction cases, a pair of contacts (12), are advantageously placed to bridge the sternum at the fourth intercostal space. Vibration is initiated at 50 Hz (or any frequency, preferably within the 20-120 Hz range), and is ideally adjusted to a maximal amplitude (or force) deemed tolerable and safe to the patient (20), preferably with the administration of thrombolytic agents or other form of drug therapy. A synergistic effect is achieved between vibration and drugs to facilitate the disruption of thromboses, relieve spasm, and restore blood perfusion.

Abstract: A multi-functional brace for a joint includes a releasable locking mechanism that allows the brace to be set for static stretch of the joint in either flexion or extension, and a range of motion assembly that allows for free movement of the joint through its natural axis over a controlled range of motion when the locking mechanism is released.

Abstract: A hinge or joint assembly is provided that includes first and second members, a pivot rotatably connecting the first and second members and allowing movement between extension and flexion positions, and at least one elastomeric spring communicating with the first and second members to restrain pivotal movement of the members toward flexion, through compression of the elastomeric spring, and to assist pivotal movement toward extension through decompression of the elastomeric spring. The assembly can further include a disk and lock slide, the disk and lock slide each having complementary teeth providing, when engaged, an arrest of pivotal movement in a direction of flexion and one-way, ratcheting, step-advance pivotal movement in a direction toward extension. The elastomeric spring can be urethane, and can be adapted to mimic any bodily muscle. An embodiment employing a torsional spring is also provided, as is a cable release mechanism providing one-dimensional cable movement.

Abstract: Knee-joint bandage of elastic textile material, the knee-joint bandage being provided with a specially shaped insert surrounding the kneecap in a cutout. The specially shaped insert being covered by an overlay of identical or similar textile material attached to the textile material with the specially shaped insert being associated with a flexible, non-expandable tensioning member. The tensioning member connecting the regions of the kneecap poles on the fibula side in an arc around the kneecap such that, when the distance between the regions increases during bending of the knee joint, the distance of the arc from the connecting line between the kneecap poles is reduced and the tensioning member presses on the adjacent side of the kneecap, medially displacing and centering the latter, wherein the tensioning member is attached to the overlay in such a manner that, during bending of the knee joint and stretching of the overlay, the tensioning member displaces the kneecap.

Abstract: An infusion device comprises a pusher for a plunger of a syringe containing a liquid to be infused. A load cell measures the push force. An encoder associated to a motor commanding the pusher measures the displacement of the pusher. A controller signals an alarm when the ratio between the variation of the push force and the displacement exceeds a predetermined threshold. The device, which serves for infusing an anticoagulant into an extracorporeal blood circuit in a dialysis apparatus, is able to signal an onset of an anomalous situation of lack of infusion in good time.

Abstract: Systems and methods separate pump the blood cells through an in-line leukofilter to a blood cell storage container. The leukofilter has a filtration medium enclosed within a flexile housing. The systems and methods can employ a fixture to restrain expansion of the flexible filter housing during operation of the pump.

Abstract: A medication dispensing apparatus with a spring-driven locking feature includes a drive member movable in a distal direction within a housing, and a fluid container with a piston that is advanceable by the drive member (60) when such drive member is moved distally by a driving means. The apparatus includes a latching element (180) having a skid (190) that is slidable along a surface of the drive member as the drive member passes distally during advancement. The drive member is arranged with the skid so as to maintain a latching lip of the latching element against a spring force in a first position free of the driving means during dose preparing and injecting prior to a final dose administration.

Abstract: An infusion device for continuous infusion of medication is disclosed, in which infusion is controlled over two separate fluid communications. The infusion is in each fluid communication controlled by restricting means and valve means, and one of the fluid communications farther contains a holding device for bolus rate of infusion for a short period. The device comprises a flow regulating device comprising a passage defined by at least a first element and a second element, wherein at least one of the first and second element is a primary deformable element adapted to be elastically deformed so as to change the cross sectional area of the passage. Furthermore the device comprises a container for storage and supply of a medication in fluid form, said container comprising a first and a second chamber being arranged relatively to each other so that when volume of the first chamber Increases the volume of the second chamber decreases.

Abstract: A membrane with at least one passage extending through an elastic material of the membrane, wherein when a cannula is inserted in the passage, the passage is expanded and the elastic material presses against the cannula and surrounds the cannula in a seal, wherein the membrane can be compressed relative to the passage, and wherein, in one embodiment, the passage exhibits a cross-sectional area having a long main axis and a short main axis perpendicular to the long main axis. The invention encompasses a membrane-cannula combination for biological and medical uses, and a membrane-connecting device combination for connecting a fluid guide and a catheter.

Abstract: A catheter system and method for intracranial infusion of therapeutic substances to a patient. An anchor formed of generally flexible, elastomeric material is used to mount the catheter to the outer surface of the skull of the patient. The anchor has a through hole for receiving the catheter, a channel, extending substantially from the through hole, into which a portion of the catheter may be inserted to retain the portion substantially parallel to the surface of the skull, and at least one flange for engaging the outer surface of the skull. An anchor clip may be provided to engage the anchor adjacent the through hole to further stabilize the catheter.

Abstract: Embodiments of the present invention regard the delivery of therapeutic. One such apparatus may comprise multiple, independently-activated, injection devices for the delivery of therapeutic or other substances. This apparatus may include a first catheter; a second catheter in the first catheter and a multiple delivery member injection device. This multiple delivery member may include an expandable member and a plurality of injection elements. A third catheter may be positioned in the second catheter. This third catheter may have a distal end connected to a wall of the expandable member and a plurality of filling tubes connected to an distal end of the third catheter. In some of the embodiments each of the injection elements may hold a pressurized therapeutic prior to release of the therapeutic.

Abstract: An ostomy appliance having a face plate assembly and inner and outer pouches joined thereto, has its outer pouch provided with one or more peripherally-extending sealing seams that allow the walls of the outer pouch to be separated by peeling forces applied in directions transverse to such seam or seams. In preferred embodiments, the sealing seam, also peelably join the peripheral edges of the outer pouch to those of the inner pouch. A method of disposing of the pouch assembly of such an ostomy appliance is also disclosed.

Abstract: A urine collection system includes a urine collection device and a suspension system. The urine collection device includes a catheter and a urine bag. The suspension system includes a waist band, an extension strap depending from the waist band, and a thigh band attached to the strap. A pair of securing straps is provided on the thigh band for securing the urine bag. A fastener is provided on the extension strap for securing the catheter and for resisting pulling by the urine bag. The catheter further includes a branch, which, along with the fastener, resists the downward motion of the catheter.

Abstract: A urine collection system includes a urine collection device and a support system. The urine collection device includes a catheter and collection component. The suspension system includes a waist band, an extension strap depending from the waist band, and a thigh band attached to the strap. A pair of securing straps is provided for securing the urine collection tubing. A fastener is provided on the extension strap for securing the catheter and for resisting movement of the catheter due to relative pulling of collection tubing or a collection bag. The catheter further includes a branch, which, along with the fastener, resists the downward motion of the catheter.

Abstract: The present invention relates to a catheter with an expandable distal end for delivering one or more medicaments. The catheter is manufactured with materials of construction that allow the transfer of electrical energy from the proximal end of the catheter to the distal expandable end. The catheter also has a means for controlling or manipulating the expandable distal end to expand and contract into various configurations. The distal end of the catheter is processed by a specific method of manufacturing whereby the expandable distal end is coated with one or more layers of a hydrogel copolymer wherein at least one layer of which coating encapsulates one or more medicaments and zero or more charged carriers to facilitate the electrophoretic and electro-osmostic mobilities of the medicaments.

Abstract: A catheter assembly with a catheter and a package for a catheter are provided. The package and catheter is provided with a seal that restricts passage of fluid between the package and the catheter. The assembly allows the catheter to be used without complete removal from the package. During urination, the assembly prevents the flow of urine from the outlet of the catheter and back through the package in a direction towards the user of the catheter. The seal allows the catheter to be dispensed from the package while the sealing is maintained and the assembly thus allows non-contaminated insertion and use of the catheter while the catheter is partly maintained in the package.

Abstract: The invention relates to a device (1) for treating human skin by means of radiation. The device comprises a housing (3) with a radiation exit opening (13). A radiation source (9) is accommodated in the housing. Radiation generated by the radiation source propagates from the radiation source towards the radiation exit opening via a radiation path (15) comprising a radiation filter having a predetermined transmission spectrum. According to the invention the radiation filter comprises a reflecting surface (23) via which the radiation propagating along the radiation path (15) is reflected. The reflecting surface has a coating which provides the reflecting surface with a reflection spectrum substantially matching the predetermined transmission spectrum. An advantage is that the reflection surface can be optimally and uniformly cooled, so that the heat generated as a result of the absorption of part of the radiation by the radiation filter can be effectively transmitted to a cooling system (25) of the device (1).

Abstract: The invention provides surgical systems and methods for ablating heart tissue within the interior and/or exterior of the heart. A plurality of probes is provided with each probe configured for introduction into the chest for engaging the heart. Each probe includes an elongated shaft having an elongated ablating surface of a predetermined shape. The elongated shaft and the elongated ablating surface of each probe are configured to ablate a portion of the heart. A sealing device affixed to the heart tissue forms a hemostatic seal between the probe and the penetration in the heart to inhibit blood loss therethrough.

Abstract: A tissue ablation system comprises a first electrode assembly adapted for insertion into a target tissue mass within a body, the first electrode assembly including a first electrode coupled to a source of RF energy in combination with an ultrasound imaging probe movably coupled to the first electrode assembly for insertion with the first electrode assembly to a desired location relative to the target tissue mass, the probe being movable relative to the first electrode assembly between an insertion configuration in which a distal end of the probe covers a distal end of the first electrode assembly and a deployed configuration in which the distal end of the first electrode assembly is uncovered.

Abstract: The invention relates to an electrosurgical instrument (5) for an endoscope or a catheter, which can be operated by means of a high-frequency current, contact electrosurgical treatment and non-contact plasma coagulation in an ionisable gas. A stationary electrode (33) is arranged on the distal end of a guiding tube (7) that can be introduced into the instrument channel (1) of an endoscope catheter (3), and when the electrosurgical electrode for the contact treatment is in the retracted position in the guiding tube (7), the stationary electrode is connected to the electrosurgical electrode (11) by means of a contact element (37).The retracted position of the electrode (11) can, but not necessarily, be maintained by an abutment (21) of a handling device (13) and/or by a suitable arrangement and measurement of the contact element (37). The retracted position of the electrode (11) does not need to be optically controlled.

Abstract: A guide element is used to guide a cutting device when removing breast tissue. The cutting device may have a tissue collection element for collecting tissue. The tissue collection element may be detachable so that the collection element may be removed independent from the cutting device.

Abstract: An electrosurgical instrument and method for treating varicose veins. In one embodiment, an elongate catheter has a distal working end that carries an electrosurgical energy delivery surface comprising at least one electrode with a positive temperature coefficient of resistance (PTCR) surface and/or an electrode with a pressure sensitive variable resistance to provide a smart surface for controlling Rf current flow at the interface of electrosurgical surface and the tissue. The electrode surface then can limit or modulate Rf energy delivery through the surface in response to the temperature of the surface or the engagement pressure of the surface against the engaged tissue. In operation, the smart electrosurgical surface prevents arcing at the electrode-tissue interface, and thus controls ohmic heating to prevent tissue desiccation, charring and emboli formation.

Abstract: A convertible threaded compression device connects a bone fragment to an anchor bone for a healing duration. The compression device has a distal bone penetration section which is advanced into the bone and a proximal bone exterior section. The proximal bone exterior section is longer than the bone penetration section. The bone penetration section includes a distal bone anchor section which threadingly engages the anchor bone, and a proximal fragment section which fits within the overbore created by the bone anchor section. A compression engagement on a distal end of the bone exterior section provides a compression shoulder. The shoulder makes substantial contact with an exterior surface of the bone fragment, biasing the bone fragment toward the anchor bone with a controlled compression force. The compression engagement enables the device to be easily removed from the healed fracture without damaging surrounding tissue.

Abstract: A surgical tool system (30) with a powered surgical handpiece (32). A removable handswitch (39) is attached to the handpiece. The handswitch includes a slip ring (192) that removably holds the handswitch to the handpiece. A lever arm (212) is pivotally attached to the slip ring. A magnet (190) is fitted in the lever arm. The angle of the lever arm is set by the surgeon to indicate the on/off state and operating speed of the handpiece. Internal to the handpiece is a sensor (94) that generates a signal based on the relative proximity of the magnet. The sensor signal is thus employed as the control signal for regulating the operation of the handpiece. Thus a surgeon can selectively use the handpiece with or without the mounted control switch.

Abstract: The present invention provides devices, systems, methods and kits for the percutaneous removal of unwanted tissue or obstructive matter from body cavities or lumens, particularly from the vasculature. Blood vessels, including the coronary, peripheral and neurovascular circulation, which are narrowed or blocked by atheromatous material or plaque are often treated with traditional endarterectomy procedures. The present invention allows the benefits of such a procedure with an intraluminal approach, particularly a percutaneous approach. Generally, the present invention provides a set of catheters or tools which are percutaneously introduceable to the site of the blockage or occlusion. The tools dissect or cut through the innermost tissue layer of the lumen to an underlying tissue layer. The innermost tissue layer is then stripped away from the underlying layer with the occlusive material thereattached.

Abstract: The present invention provides medical devices comprising nanomaterials. By utilizing nanomaterials in the production thereof, the inventive medical devices can be provided with various advantageous properties and/or capabilities. Methods of producing the inventive medical devices are also provided. Inasmuch as the inventive devices are expected to provide certain advantages in their use, there is also provide a method of medical care, including methods of treatment or diagnosis, wherein the inventive devices are brought into therapeutic contact with a body to be treated or diagnosed thereby.

Abstract: The invention relates to a medical instrument having a hollow shaft (2) and, positioned on its proximal end, a handle (3) consisting of at least two gripping members (3a, 3b) and, on its distal end, a tool consisting of at least two jaw members (5a, 5b). The instrument's jaw members (5a, 5b) are stationed at a lateral angle to the longitudinal axis of the shaft (2) so that at least one jaw member (5a) of the tool (5) can be moved for opening and closing by means of a gripping member (3b) of the handle (3) that can be rotated with respect to the at least one other jaw member (5b) of the tool (5) and the at least one movable jaw member (5a) and the corresponding gripping member (3b) of the handle (3) serving to move the jaw member (5a) are connected to one another by a compression-tension element (8) positioned in the hollow shaft (2).

Abstract: Masses of particles are structurally supported by the application of vacuum through a support surface having holes thereon that are smaller than the average diameter of the particle mass that is to be supported. The reduced pressure structurally supports particles on the support surface. The mass of particles tends is so well supported that it tends retain its shape unless additional forces are applied. The system comprises the vacuum applicator (e.g., pump), a vacuum carrying system and the support surface. When a mass of particles is supported on the support surface under vacuum, the particles can be carried to a target surface, the mass of particles pressed against the target surface, the mass conforming to the target surface, and the vacuum reduced or stopped, depositing the particle mass onto the surface in excellent shape compliance with that surface.

Abstract: The present disclosure relates to surgical instruments including a staple anvil formed in a distal end of the surgical stapler and a staple cartridge selectively receivable in a distal end of the surgical stapler and in juxtaposition relative to the staple anvil, the staple cartridge including one or more laterally spaced apart rows of staple slots formed in an upper surface thereof, a plurality of surgical staples disposed, one each, within the staple slots, and a staple line reinforcing system configured and adapted to augment the strength of the staple line formed by the firing of the surgical staples into body tissue, wherein the surgical stapler concomitantly drives the plurality of surgical staples through the adjacent layers of body tissue to mechanically secure the body tissue and activates the reinforcing system to non-mechanically secure the adjacent layers of body tissue to one another.

Abstract: A suture anchor that allows a surgeon to securely and efficiently suture soft tissue to bone without knotting the suture, comprising a locking body through which a suture is passed, and an anchor collar, which, when positioned over the suture passing through the locking body, secures the suture.

Abstract: A metallic inverted L-shaped implant is used to resurface the superior facet of the inferior vertebrae limited to the facet joints located on the spine, Occiput-C1 through L5-S1. The metallic implant is highly polished on its exterior and textured on its interior surface. It is mechanically crimped in place without the use of cement or pedicle screws. Permanent fixation occurs when bone in-grows onto a rough, porous surface on the inside of the implant. The implant employed in a hemi-arthroplasty method resurfaces half of the facet joint to provide for smooth, pain free joint articulation in deteriorated or diseased spinal facet joints without the need for major surgery or rehabilitation at considerably less risk to the patient.

Abstract: A vertebral rod assembly comprises first and second members that may rotate about a first axis. Each of the first and second members includes a base and a vertebral support rod extending from the base. An extension extends from the base on the first member into an opening formed in the base of the second section. A fastener extends through the base of the second member to lock the first and second members, and to prevent the rotation of the first member and second member.

Abstract: A convective warmer to which blankets of different dimensions may be connected is capable of providing air to the various blankets at flow rates that optimally inflate those blankets to achieve the optimal clinical result for the patients covered by those blankets. The blanket connected to the warmer may range from a full size adult warming blanket to a pediatric or neonate warming blanket. There is provided on each blanket a code, marking or marker, to be read by a sensor(s) provided at the outlet of the warmer, that identifies the type of blanket when the blanket is coupled to the warmer. Consequently, heated air may be automatically output by the warmer to the blanket at the appropriate flow rate of that blanket to optimally inflate the blanket without any need for intervention by a user. In addition to being used to control the flow rate of the heated air, the code from the blanket may also be used to control the temperature of the heated air to be input to the blanket.

Abstract: A stent delivery system a catheter has an axially extending inner core and outer sheath. Axially spaced rings extending from a relatively narrow diameter portion of the inner core proximate the distal end thereof. The rings engage proximal portions of a compacted stent disposed within the sheath and over the core and rings. A proximal handle of the system has a first portion that supports the sheath and a second portion that supports the core for relative displacement of the core and the sheath. Retraction of the sheath relative to the core uncovers the stent engaged by the rings which tends to remain stationary relative to the core so that upon partial retraction of the sheath a distal end of the stent expands to its expanded form. Further retraction of the sheath deploys the stent, retracting the core returns the distal portion of the stent into the sheath.

Abstract: The present invention relates to implantable medical devices for the localized delivery of therapeutic agents, such as drugs, to a patient. More particularly, the invention relates to a device having a gradient of water soluble therapeutic agents within a therapeutic agent layer and a mixing layer that allows for controlled release of the therapeutic agents.

Abstract: This invention relates to an intervertebral motion disc having two motion surfaces and an open channel.

Abstract: A prosthesis (20) for use in performing joint arthroplasty is provided. The prosthesis (20) is to be fitted to a long bone (3). The prosthesis includes a first body (22) having a first body articulating surface (24) defining a generally circular outer periphery (26) of the first body articulating surface (24). The first body (22) has a support surface (28) opposed to the articulating surface (24). The support surface (28) is adapted to receive the head of the long bone (3). The prosthesis (20) also includes a second body (30) operably associated with the first body (22). The second body (30) has a second body articulating surface (32) extending from a portion of the circular outer periphery (26) of the first body articulating surface (24).

Abstract: A replacement device for resurfacing a joint surface of a femur and a method of making and installing such a device is provided. The custom replacement device is designed to substantially fit the trochlear groove surface, of an individual femur. Thereby creating a “customized” replacement device for that individual femur and maintaining the original kinematics of the joint. The replacement device may be defined by four boundary points, and a first and a second surface. The first of four points is 3 to 5 mm from the point of attachment of the anterior cruciate ligament to the femur. The second point is near the bottom edge of the end of the natural articulatar cartilage. The third point is at the top ridge of the right condyle and the fourth point at the top ridge of the left condyle of the femur.

Abstract: A multiuse laundry cleaning device in a solid state containing a homogeneous quantity of cleaning agent configured to dissolve and release a substantially consistent quantity of cleaning agent over a plurality of laundry wash and rinse cycles. The cleaning agent includes a gas-releasing component, potassium silicate as a solubility control component to limit the solubility of the cleaning agent, an alkalinity agent as a pH regulator, and a water softener to solvate metal ions in a solution of water. Controlled dissolution of the cleaning agent composition releases a desired quantity of cleaning agent in each cleaning cycle over a plurality of cycles. A porous covering of bag may be disposed around the solid cleaning agent.

Abstract: Cationic naphthyldiazo dyes of general formula (I) and colorants for keratin fibers containing these dyes.