System for preventing bacterial infections in needle trajectories. The system includes a percutaneous surgical instrument (1) percutaneously introducible into a patient's tissue (3) such as a biopsy needle, and having an outer surface made of an electrically conductive material; a contact electrode (4) applicable to the patient's skin (3a); a silver coating or element (P) arranged on or forming part of the instrument (1) to break down by electrochemical release when a current is applied thereto, releasing silver ions into its surroundings; and an electric current generator (2) arranged and configured for generating a current and inducing the temporary circulation thereof between the instrument (1) acting as an anode, the tissue (3) and the contact electrode (4) acting as a cathode, respectively, with a specific magnitude and duration for producing a massive and sudden release of silver ions for the purpose of preventing post-treatment bacterial infections.

An apparatus and a method for analysing samples taken by biopsy, which make it possible to perform the analysis of these samples whilst the patient is still positioned in the position for taking samples, in such a way as to make the overall procedure for taking and analysing the samples faster, reducing the inconvenience for the patient and the risk of a new examination, and also reducing in the majority of cases exposure of the patient to X-rays.

Various systems and methods are provided for surgical and interventional planning, support, post-operative follow-up, and functional recovery tracking. In general, a patient can be tracked throughout medical treatment including through initial onset of symptoms, diagnosis, non-surgical treatment, surgical treatment, and recovery from the surgical treatment. In one embodiment, a patient and one or more medical professionals involved with treating the patient can electronically access a comprehensive treatment planning, support, and review system. The system can provide recommendations regarding diagnosis, non-surgical treatment, surgical treatment, and recovery from the surgical treatment based on data gathered from the patient and the medical professional(s). The system can manage the tracking of multiple patients, thereby allowing for data comparison between similar aspects of medical treatments and for learning over time through continual data gathering, analysis, and assimilation to decision-making algorithms.

A biological sample collection system can include a sample collection vessel having a closed first end and an open second for receiving a biological sample. The system can additionally include a sealing cap configured to associate with the sample collection vessel, a reagent chamber secured within an interior space of the sealing cap and retaining a measure of sample preservation solution, a shim circumferentially associated with a proximal end of the reagent chamber and spanning the distance between the reagent chamber and the interior sidewall of the sealing cap, and a plug having a diaphragm configured to selectively engage the shim and form a seal for retaining the sample preservation solution within the reagent chamber. Associating the sealing cap with the sample collection vessel displaces the diaphragm from the shim and breaks the seal formed therebetween, opening a fluid path between the reagent chamber and the sample collection chamber.

Discloses is a system for the wireless transmission of energy and/or signals between spatially-separated regions with no electrically-conductive connection, the conversion of energy and/or signals into other forms of energy and/or forms of signal, and the application and/or detection of same in at least one peripheral region of said system. The system allows a wireless transmission of energy between at least two spatially-separated regions without an electrically-conductive connection, energy being supplied to at least one of these regions, transmitted to at least one additional region in a wireless manner, converted on demand into other forms of energy, and applied in a peripheral region of said system. Signals can be transmitted at the same time as energy is being transmitted.

A guide device for guiding a medical instrument relative to a patient. The guide device is usable with a first plate including a plurality of apertures. The guide device includes a body, a plurality of outer passageways, and a flexible member. The body is defined by at least one surface that includes a generally proximal portion and a generally distal portion. The plurality of outer passageways extend from the generally proximal portion through the body to the generally distal portion. A flexible member is disposed between each passageway. The flexible member defines an inner passageway and is selectively deformable such that a selected passageway of the plurality of outer passageways or the inner passageway is configured to receive at least a portion of the medical instrument.

A biopsy device includes a body, a needle, a cutter, and a tissue sample holder. The needle extends distally from the body. The cutter is longitudinally translatable relative to the needle and defines a cutter lumen. The tissue sample holder includes a rotatable member, an individual sample tray, and one or more bulk sample trays. The rotatable member defines a single chamber partially divided by a plurality of tray protrusions extending radially inwardly from a cylindrical wall of the rotatable member. The individual sample tray includes a single sample chamber that is configured to receive a single tissue sample. The bulk sample tray is configured to receive a plurality of tissue samples.

A biopsy device includes a body, a needle, a cutter, a tissue sample holder, and a gate assembly. The needle extends distally from the body. The cutter is longitudinally translatable relative to the needle and defines a cutter lumen. The tissue sample holder is coupled proximally relative to the body. The cutter lumen of the cutter defines at least a portion of a fluid conduit extending between the cutter and the tissue sample holder. The gate assembly is configured to selectively arrest movement of a tissue sample holder within the fluid conduit between the cutter and the tissue sample holder.

Various systems and methods are provided for surgical and interventional planning, support, post-operative follow-up, and functional recovery tracking. In general, data related to retraction of tissue can be gathered during performance of a surgical procedure. In one embodiment, the data can be used during performance of the surgical procedure, e.g., to determine whether a length of time a tissue is retracted using a retractor reaches a predetermined threshold amount of time, an amount of tissue retraction reaches a predetermined amount of tissue, and an amount of pressure being placed on tissue and/or nerves as a result of retraction reaches a predetermined amount of pressure, and/or the data can be used after performance of the surgical procedure, e.g., in determining a correlation between the data and patient pain level data.

A testing device for body fluid analysis includes: a sheet unit having a sheet of which a first surface receives body fluid of a user to be deposited thereon; a contact unit having a magnifying lens group for magnifying the body fluid deposited on the sheet, the contact unit being provided with a first side at which the magnifying lens group is placed to face the first surface of the sheet and being provided with a second side at which a guide facing an observation means is placed; and a light source unit placed to face a second surface of the sheet unit in a direction facing the contact unit with the sheet unit in between, the light source unit having a light source providing light to the sheet unit.