An intraocular shunt can be placed into the eye in an ab externo approach. A clinician may determine an entry area below a corneal limbus of an eye and a target outflow region. Thereafter, the clinician can insert a hollow shaft into the eye at the entry area toward an anterior chamber of the eye, the shaft carrying an intraocular shunt therein. The clinician can position an inflow end of the shunt within the anterior chamber of the eye and, while maintaining the shunt inflow end in the anterior chamber, can remove the shaft from the eye to release the shunt. Finally, the clinician can repositioning an outflow end of the shunt within the target outflow region and verify placement of the outflow end of the shunt within the target outflow region.

A modular IOL system including intraocular primary and secondary components, which, when combined, form an intraocular optical correction device, wherein the secondary component is placed on the primary component within the perimeter of the capsulorhexis, thus avoiding the need to touch or otherwise manipulate the capsular bag. The secondary component may be manipulated, removed, and/or exchanged for a different secondary component for correction or modification of the optical result, on an intra-operative or post-operative basis, without the need to remove the primary component and without the need to manipulate the capsular bag. The primary component may have haptics extending therefrom for centration in the capsular bag, and the secondary component may exclude haptics, relying instead on attachment to the primary component for stability. Such attachment may include actuatable interlocking members.

An ocular medical injector is provided for drug delivery. A method includes inserting a puncture member of the medical injector into the eye until the puncture member reaches the SCS. The puncture member defines a lumen therethrough. With the puncture member disposed within the SCS, a flexible cannula is advanced distally through the lumen of the puncture member, beyond the distal end portion of the puncture member and along the SCS towards a posterior region of the eye. The flexible cannula has an atraumatic distal tip and defines a lumen therethrough. With the distal tip of the flexible cannula disposed within the SCS beyond a distal end portion of the puncture member, a therapeutic substance is administered to the SCS.

Multi-functional foot controller with treadle for controlling a first function and as an integrated shroud for a switch that controls an additional function.

The present invention relates to an ophthalmic knife and methods of its use for treatment of various conditions including eye diseases, such as glaucoma, using minimally invasive surgical techniques. The device is configured for cutting the tissues within the eye, for example, a trabecular meshwork (TM).

A cartridge for a panel of an ophthalmic surgical system for treating an eye is configured for insertion in a cartridge accommodation region of the panel and has at least one fluid pump for conveying a treatment fluid, the fluid pump has a pump chamber and a drive chamber separated from the pump chamber with a partition element that is at least regionally deflectable, wherein a drive fluid is feedable to the drive chamber and the treatment fluid is feedable to the pump chamber. The partition element has at least one plate element made of an at least electrically conductive or at least ferromagnetic material, said plate element also being deflected in the case of a deflection of at least one region of the partition element. Further, a panel and an ophthalmic surgical system are provided.

A cassette for a console of an ophthalmosurgical system for treating an eye is configured for insertion into a cassette receiving region of the console and has a fluid pump configured to deliver a treatment fluid, a tube for attachment to a handpiece, and a connection unit secured against detachment, of a cassette-side end of the tube to a cassette housing of the cassette. The connection unit includes an attachment stub arranged on the cassette housing and has a through opening for the treatment fluid, and a plug-in connector arranged on the cassette-side end of the tube and likewise has a through opening for the treatment fluid, with the plug-in connector, when it is connected to the attachment stub, being held in a fluid-tight manner with respect to the attachment stub and so as to be able to rotate about a longitudinal axis of the through opening.

A console for a medical treatment system includes a console housing and a control unit for controlling a medical treatment instrument. A foot-operated control unit wirelessly coupled to the control unit, and the console housing has at least one side wall, which has a bearing surface for arranging the foot-operated control unit in a not-in-use position. The bearing surface is inclined with respect to a horizontal plane, at least in the region where the foot-operated control unit is arranged, in order when arranging the foot-operated control unit on the bearing surface to bring about bearing of the foot-operated control unit against the bearing surface by the weight of the foot-operated control unit. The side wall has in the region of the bearing surface a console-side connecting unit for releasably connecting the foot-operated control unit to the console. Further, a corresponding foot-operated control unit and a medical treatment system are provided.

A tube for a medical treatment system has a first channel for feeding an irrigation fluid from a console of the system to a medical treatment instrument of the system and a second channel for discharging an aspiration fluid from the instrument to the console. The first and the second channels are arranged in parallel. The first channel has a first wall and the second channel has a second wall. A second material of the second wall has a greater hardness than a first material of the first wall. The tube is formed from two individual tube elements for the channels. The tube elements are welded or adhesively bonded in a connection region. The difference between the hardness of the first material and the hardness of the second material is at least 10 ShA and at most 15 ShA.

A method for identifying saline solution in an aspirated fluid mixture during vitrectomy or another vitreoretinal surgery includes estimating a fluid property value of the mixture via an electronic control unit (ECU). The mixture includes saline solution and either vitreous or silicone oil. The method includes identifying the saline solution as a primary constituent fluid of the fluid mixture, via the ECU, based on the fluid property value, and activating an indicator device in response to the primary constituent fluid being the saline solution. An automated system for identifying saline solution in the aspirated fluid mixture includes the indicator device and the ECU. A computer-readable medium includes instructions, executable by a processor to identify an aspirated fluid mixture during a vitreoretinal surgery, with execution of the instructions by the processor causing the processor to perform the method.