This invention relates to the field of assisted—and even automated—manipulating of instruments or tools, or more generally elongated pieces or objects, in particular in applications that require high precision and maximum safety, such as that of surgical interventions on living subjects or actions that take place close to a man, and even in interaction with him.
In these contexts, the invention has as its object a pneumatic device for holding and moving an elongated object, a medical or industrial system that integrates at least one such device, and a method for inserting an elongated object via such a system.
In numerous technical fields, there is a need for automatic or semi-automatic devices that make it possible to move an elongated element or piece gradually, in particular for the purpose of inserting it into a body or another element.
This is true in particular for the medical field and more specifically surgery.
Already, a substantial number of robotic devices are being proposed for assistance with medical and surgical motions. For many of them, the robotic system is designed for the manipulation of tools such as surgical instruments, in particular in the form of elongated bodies, or needles in the case of, for example, interventional imaging.
In minimally invasive surgery, the fact that they traverse trocars determines the shapes and designs of tools and instruments that are used and limits the number of independent movements that can be performed. The translational movement along the axes of the tools, of oblong geometry, is then very heavily stressed.
In the same way, percutaneous procedures, which consist in inserting needles or analogous medical tools for getting into an area of interest, require a translational movement of needles of broad amplitude, which movement has to be carried out with a very high level of safety.
Within all of these contexts, if the oblong and elongated geometry of the objects that are to be moved is a constant, the diameters of their generally cylindrical bodies can widely vary, even during the same motion. It is the same with their length.
Most of the existing solutions are based on actuating systems that are integral with the tool that entails a modification of the standard tool (which is not desirable). The translational movement is generally carried out via a transformation of movement (passage from a rotational movement to a translational movement in particular). If need be (breakdown, medical emergency), the decoupling between the tool and the feed system is quite complex and can involve the safety of the patient. Furthermore, the increasingly widespread use of imagers (echography, fluoroscopy, X scanner, MRI) when the motion is being carried out makes it difficult and even impossible to employ a number of actuating technologies that are currently in use.
Various known techniques for assisted movement, motorized or mechanized, of the step-by-step or sequential type apply the so-called kinematic principles of the caterpillar (“inchworm” in English), in particular with regard to the components that can be inflated or actuated pneumatically.
Various implementations of these principles have already been proposed in the medical and surgical field, either to allow the at least partially automated advancement of an elongated object (for example, an endoscope) in a subject's natural conduit (see, for example: US 2010/022947; EP 1 792 561; U.S. Pat. No. 5,398,670; WO 02/068035), or to move, from the outside and in a partially automated way, at least one elongated object that has to be inserted into the body of a subject (see, for example: WO 2014/068563).
However, these known embodiments using an “inchworm”-type kinematics have at least some of the drawbacks below: complex structure; significant axial bulk; multiple constituent components; incompatibility with certain medical imaging technologies; limited adaptation to objects that have variable diameters or different values; use of various types of energy.
In addition, these embodiments all have the common drawback, on the one hand, of requiring several, i.e., at least two, feed lines for the various active components of the moving devices, on the other hand, of having to guide the various lines in a synchronized manner (difficult to accomplish when said lines are of significant lengths), and, finally, of having limited ability to adapt how said active components of the device engage with the elongated object that is to be moved.
Another field in which there is a growing need for preferably automated or at least semi-automated devices is that of the operating contexts and environments in which a motorized or actuated device is to operate in interaction with a human operator, by imitating or by assisting the motion of such an operator or else the environments with tight constraints, excluding in particular the use of electromechanical, electrotechnical or electronic technologies.
Thus, it is possible to cite the case of tasks of assembling mechanical components on assembly lines, where so-called collaborative robots for assisting the operator are now being proposed. For these devices, weight is a risk factor in the event of a collision. The existence of inherent flexibility to which one skilled in the art refers as compliance is a property that is furthermore important for managing the robot/operator contact. Finally, it is necessary to propose robots of minimum size so as not to hamper the operator in his movements and his collaboration with the robot.
In an industrial setting, it is also possible to cite automated tasks of the so-called “peg-in-hole” type (“plug in hole” or “plug-in” hole) in which the motions of assembling mechanical components are carried out. The assemblies are often based on centering elements for referencing the positions of the elements. It is possible to cite the context of the automobile, for example, with the assembly of engine components, or the insertion of electrical connectors in the electrical and electronic industry. It is known that a rigid hold of the two elements that are to be assembled does not make possible the success of a robotized assembly. It is often necessary to use at least limited compliance in directions that are perpendicular to the axis of insertion.
Furthermore, in the context of the collaborative handling, the safety of the human operator is of paramount importance. To ensure his safety, it is necessary not only to monitor the speed of the robotic system but also the motive forces that it exerts.
The existing technologies of the type called “artificial muscle” make it possible to respond at least in part to the problems and needs expressed above.
However, they are very difficult to implement and control, require difficult and tedious assemblies, and absolutely must be combined with additional kinematic guide means.
Finally, there are also industrial contexts where the environmental constraints are stringent and exclude the use of electromechanical technologies. These include, for example, the case of explosive environments, because of the handling of inherently dangerous products (explosive materials), or under specific conditions, such as, for example, the handling of powders as used in fields such as additive manufacturing. In this case, the use of technologies eliminating any active element on an electrical plane is a certain advantage.
This invention has as its object to propose a solution that makes it possible to overcome at least some of the drawbacks and the primary above-mentioned limitations.
For this purpose, it has as its object a pneumatic device for holding and moving an elongated object, with said device comprising a hollow body of general annular or tubular shape defining an axial direction, traversed by the elongated object at an axial passage and consisting of two end parts or segments arranged in a manner that is aligned in the axial direction and that forms jaws and a median or central part or segment that connects the two parts or segments that form jaws with one another, with relative ease of movement of one in relation to the other in the axial direction under the action of a controlled deformation of at least one portion of said median or central part or segment,
device characterized in that the various parts or segments of the hollow body define respective chambers,
in that the end part(s) or segment(s) that form jaws comprise elastically deformable membranes as wall portions that are designed to come into contact with the elongated object in the clamping phase,
and in that the chambers of the two end parts or segments are in fluid communication with the chamber of the median or central part or segment, each via at least one respective calibrated flow means, with the injection of pressurized gaseous fluid being carried out by means of a single feed line that is connected to a controlled source of pressurized fluid and that empties into the chamber of one of the two end parts or segments, based on the direction of translational movement that is desired for the elongated object that is present in the hollow body.
The invention will be better understood owing to the description below, which relates to preferred embodiments, provided by way of non-limiting example and explained with reference to the accompanying diagrammatic drawings, in which:
This device 1 comprises a hollow body 1′ of general annular or tubular shape that defines an axial direction DA, traversed by the elongated object 2 at the level of an axial passage 4, and consists of two end parts or segments 5 and 5′ that are arranged in an aligned manner in the axial direction DA and that form jaws and a median or central part or segment 6 connecting the two parts or segments that form jaws 5 and 5′ with one another, with relative ease of movement of one with regard to the other in the axial direction DA under the action of a controlled deformation of at least one portion 14, 15′ of said median or central part or segment 6.
In accordance with the invention, it is provided:
that the various parts or segments 5, 5′, 6 of the hollow body 1′ define respective chambers 7, 7′, 6′,
that the end part(s) or segment(s) 5, 5′ that form jaws comprise elastically deformable membranes as wall portions 8, 8′ designed to come into contact with the elongated object 2 in the clamping phase,
and that the chambers 7, 7′ of the two end parts or segments 5, 5′ are in fluid communication with the chamber 6′ of the median or central part or segment 6, each via at least one respective calibrated flow means 9, 9′, with the injection of pressurized gaseous fluid being performed by means of a single feed line 10, 10′ connected to a controlled source of pressurized fluid 11 and emptying into the chamber 7, 7′ of one 5 or 5′ of the two end parts or segments 5, 5′, based on the direction of translational movement that is desired for the elongated object 2 that is present in the hollow body 1′.
As
The end parts or segments 5 and 5′ then have a concentric arrangement seen in the direction DA.
Consistent with a design variant of the invention, illustrated diagrammatically in
The median or central chamber 6′ may or may not share common walls with the terminal chambers 7 and 7′.
The gaseous fluid is preferably air under low pressure (preferably 1 to 5 bar), optionally treated, easily available in health establishments or industrial sites.
The elongated object 2 can consist of, for example:
For its handling by the device 1, the object 2 is to comprise at least one elongated part of cylindrical shape if it does not have a cylindrical elongated design overall.
Thus, the invention provides a device 1 that forms a linear actuator for any type of elongated piece, instrument or tool 2, with the ability (owing to the surface contact of the membranes 8, 8′) to grasp pieces, tools or instruments of various sizes and diameters firmly, without the latter having to undergo any modification (for achieving possible cooperation, a hypothetical coupling or interlocking) and without their outside surface being modified or degraded by their use with regard to the device 1.
The axial through passage 4 is advantageously sized based on larger tools or instruments 2 provided for handling by the device 1 (objects or pieces of larger diameters).
With the movement not being carried out with a continuous motion but in a sequential manner, the risks of uncontrolled movement and even of undesirable movement are limited (in frequency and in scale), and even eliminated. The safety of the motion, within a medical context, is therefore greatly increased. In addition, taking into account forces in play and the speed of execution of the successive elementary motions, a dominant and corrective human intervention is always possible.
In addition, taking into account the enveloping structure of the hollow body, or at least of the two end jaws 5 and 5′, around the oblong object 2 that is to be moved, holding the latter in a tube with a specified diameter is always ensured, while allowing freedom of movement framed in this cylindrical interior volume (axial passage 4). Actually, in the deflated state or at rest, the device 1, with its tubular passage 4 in which the tool or instrument 2 is placed, prevents too significant a displacement in relation to the axial direction DA, but allows a sufficient motion that makes it possible, for example, for a surgical needle that is planted in an organ to follow the physiological motion of the latter (rotational motion of the needle in relation to its point of insertion in the body of the subject 19) or else to be manipulated by the practitioner.
Furthermore, and consistent with a significant advantage provided by the invention, the feeding by a single line 10, 10′ (by direction of movement) greatly simplifies the connector, reduces the space requirement at the site for implementing the device 1, and facilitates the management of the fluid. Actually, the various consecutive kinematic stages that are necessary for achieving the movement of the object 2 by successive elementary steps are carried out naturally and without active intervention other than the injection and the stopping of the injection of pressurized fluid, because of the particular calibrated communication of the three chambers 7, 6′ and 7′ that determines the order, the duration and the intensity of the activation sequences (pressurization) and deactivation (depressurization) of the latter generating an “inch-worm”-type movement.
Finally, taking into account its pneumatic and structurally deformable nature, the device 1 in all of the circumstances of implementation (even inflated) has an at least minimum axial and/or radial compliance.
Advantageously, the end parts or segments 5, 5′ that form pneumatic jaws, respectively front and rear based on the direction of positive movement of the elongated object 2, delimit chambers 7, 7′ that are annular or rotationally toroidal in shape around the axial direction 41 DA and that have a structure that is essentially non-deformable—axially and radially—within the range of operational pressures of fluid that is injected during normal operation of the device 1, with the exception of elastically deformable membranes that form internal sleeves 8, 8′ that constitute through housings of the jaws for the elongated object 2, forming by alignment the axial passage 4 of the multi-chamber hollow body 1′.
Thus, the device 1 comprises two annular or toroidal chambers with an elastically deformable wall 8 or 8′, under internal pressure, radially toward the inside (pneumatic jaws function) and a median annular or tubular connecting chamber 6′, elastically deformable under internal pressure by axial elongation or extension of the hollow median segment 6 that delimits it.
Preferably, the median or central part or segment 6 has at least one common wall portion 12, 12′ with respectively each of the two end parts or segments 5, 5′, with each of said common wall portions 12, 12′ thus participating simultaneously in the partial delimitation of one of the terminal chambers 7, 7′ and with that of the median or central chamber 6′. In this case, the calibrated flow means 9, 9′ can consist of through holes that are made in said common wall portions 12, 12′ and that have specified shapes and sizes, based on the desired sequencing for the inflation and the deflation of the chambers 7, 6′, 7′ determining the amplitude and/or the speed of the translational movement of the elongated object 2 in question.
Consistent with a characteristic of the invention, the calibration of each of the respective flow means 9, 9′ between each of the terminal chambers 5, 5′ and the median or central chamber 6, which is optionally different and suitable for each means 9, 9′, is adjusted in such a way that, by passive monitoring of the circulation of the gaseous fluid that is injected via the single feed line 10, 10′, the two terminal chambers 5 and 5′ can be under an operational pressure that brings about an effective double clamping of the object 2 that is to be moved, when the median or central chamber 6 is under operational pressure and in its deformed state.
One skilled in the art understands that the passive monitoring of the flow of gaseous fluid between the various communicating chambers 6′, 7, 7′—both during the injection phases (inflation) and during the evacuation phases (deflation)—primarily depends on the sizing of the means 9 and 9′, namely the diameter of each of the holes 9 and 9′ within the framework of the preferred variant embodiment of the invention. These monitored flows that are determined by sizing at manufacture define the durations of inflation and deflation sequences of the chambers 6′, 7, 7′ during the two phases, with regard to, of course, the volumes of said chambers and their coefficient of expansion by deformation, with the pressures/negative pressures applied, with the nature of the gaseous fluid that is used (normally air), and with the mutual cyclic ratio of the inflation and deflation phases.
Another parameter of importance is the clamping force that is desired at each jaw 5, 5′.
For a device 1 as shown in
A simulation based on the laws and rules of fluid mechanics and the elastic deformation of the bodies, easily within the scope of one skilled in the art, may make it possible to size the device 1 and its operating parameters based on the desired operational result.
The chronologically successive stages of a kinematic cycle of the device 1 as it is shown in
The above-mentioned cycle described with regard to the representations of
When, for example in the case of a depression with elastic return or resistance to the depression, the goal is to maintain a continuous grip during the entire depression motion, the cyclic ratio between the two phases can be modified (for example, 70/30) in such a way that the inflation of the front jaws 5 begins before the deflation of the rear jaws 5′ is achieved, and even before it has begun. In this case, the device 1 is engaged permanently with the object 2 during the entire movement by cyclic pitch of the latter.
So as to amplify the elongation phenomenon of the median or central part 6 and consequently the movement step per kinematic cycle, it may be provided that this part 6 is at least partially formed by or covered with a layer 13 of an auxetic material, i.e., with a negative Poisson's ratio. The auxetic nature of said material can originate from the structure of the latter and/or the very nature of said material.
In accordance with a preferred practical variant embodiment, the multi-chamber hollow body 1′ with its three outputs or segments 5, 5′ is entirely made of polymer material(s), preferably both as a one-part piece, or made integrally, for example by three-dimensional printing, with the deformable membranes 8, 8′ of the jaws 5, 5′ optionally being connected by over-molding of a specific distinct polymer material.
Thus, the device 1 can be used in any context of medical imaging and can be manufactured for a low cost, optionally in the form of a disposable product.
In an advantageous manner, nevertheless, the polymer materials that are used, for example rigid acrylate resin (of an elasto-plastic nature) for the rigid walls of the hollow body 1′ and flexible acrylate resin (of an elastomeric nature) for the elastically deformable walls of the latter, are of a nature to withstand sterilization and are compatible with use in a sterile chamber.
As a variant, the rigid material can be a polypropylene or a polyoxymethylene, and the flexible material can be a silicone.
The walls of the hollow body 1′ can also be produced from an alloy with shape memory, optionally with a specific configuration of said walls, for a deformation that is controlled and reversible based on the internal pressure in the chambers 6′, 7, 7′. An elastically flexible material can be connected by over-molding to form the membranes 8, 8′.
For the purpose of using a device 1 that can move the elongated object 2 both ways in the axial direction DA, without modifying the mutual arrangement thereof, and therefore being able to concatenate insertion and extraction motions, it can be provided that a conduit 10, 10′ that is able and is designed to form selectively a feed line or a drain line is connected to each of the chambers 7, 7′ of the end parts or segments 5, 5′ (
According to a first embodiment of the invention, illustrated in
In this embodiment, the device 1 at rest has a longitudinal extension in the direction DA of minimum value, for a contact surface of the jaws 5, 5′ with the object 2 that is maximum.
Actually, the median part 6 and its associated chamber 6′ extend around jaws 5 and 5′ and have an axial dimension that is less than the total of the axial dimensions of the two jaws 5 and 5′. Thus, at rest, the axial dimension of the device 1 corresponds to the sum of the axial dimensions of the two jaws 5 and 5′, which are in contact axially.
In accordance with an advantageous practical design with regard to the first above-mentioned embodiment, the median or central part or segment 6 of the multi-chamber hollow body 1′ consists of, on the one hand, a portion of internal tubular wall 14 that can be deformed elastically in the axial direction DA and that connects the two end parts or segments 5, 5′ between them, and, on the other hand, an outside wall portion with a U-shaped cross-section 15, for rotation around the axial direction DA and that forms—by additionally cooperating with the portion of internal tubular wall 14—the annular or toroidal median or central chamber 6′ of the hollow body 1′, with the two wings 15′ of the U also being connected by their free ends to the two end parts or segments 5, 5′ and being elastically deformable by bending toward the outside of the U in the axial direction DA, under the action of an adequate overpressure in the central or median chamber 6′.
The inflation of the median or central chamber 6′ consequently brings about an elastic spacing of the wings 15′ of the rotational structure with a U-shaped cross-section 15 and simultaneously an elastic stretching of the internal tubular wall 14 in the axial direction DA, producing a spacing of the two end parts or segments 5 and 5′ between them.
Based on the desired kinematics, one of the two wings 15′ (for example, the front wing 15′ that is associated with the end part 5) can have greater deformability and can even be the only deformable wing. A simultaneous elastic deformation of the front and rear wings 15′ makes it possible to increase the cyclic pitch of the device 1 (see
The median or central part or segment 6, in addition to defining a central or median chamber 6′ that expands under pressure, produces a double elastic bond between the two end parts or segments 5 and 5′.
The openings 9 and 9′ for fluid communication are made in the wall portions 12 and 12′ that are located between the wings 15′ and the sites for making the tubular wall 14 integral with the end parts or segments 5 and 5′, at the rigid walls of the latter that form the annular chambers 7 and 7′ with the membranes 8 and 8′.
For the purpose of optionally producing a more significant movement in each cycle, the areas 15″ of the outside wall portion with a U-shaped cross-section 15 that correspond to the wings 15′ of said U are formed by or covered with, preferably on their internal face, a layer 13 made of auxetic material (
By way of practical example of the design of a device 1 that is produced by the inventors, on the basis of the embodiment that is shown in
By designing and by using a device 1 that is sized as indicated above and by modeling its behavior, the inventors have been able to establish the curves of
According to a second embodiment of the invention, as shown in
In accordance with an advantageous practical design, the elementary formations 17 together constitute a network 16′ with an inverted honeycomb pattern and are arranged in several consecutive rows in the direction DA.
When a more complex motion than a simple translational movement is sought, it can be provided, for example, that at rest, the auxetic network 16′ is twisted around the axial direction DA, with an operational pressurization of said network bringing about a relative translational movement and a relative rotational movement between the two end parts or segments 5 and 5′ (
Consistent with another design variant of the invention, illustrated in
Within the framework of this design variant, it can be provided that a first of the two functional chambers 22 is configured to ensure a rotational movement around the axial direction DA of the elongated element 2 that is clamped by one 5 of the two end jaws 5, 5′ and that the second of the two functional chambers 22′ is configured to ensure a translational movement in the axial direction DA of the elongated object 2 that is clamped by the median jaw 23 and the other end jaw 5′.
The resulting sequenced motion is shown in
Such a double device 1 functionally and structurally corresponds to the agglomeration of two devices 1 that are coupled axially (one for the rotation and one for the translation), with the central jaw 23 being shared and common to both.
So as to be able to vary in particular the cycle durations and/or the speeds of certain optional phases, the device 1 can comprise, as
Advantageously, the or each adjustment means 25, with manual or motorized actuation, comprises a movable variable sealing element of the calibrated opening 9, 9′, 24, 24′ that forms the flow means in question.
The above-mentioned adjustment can be done at the beginning of the cycle and can be constant during the cycle or during two phases of the same cycle.
As shown diagrammatically in
This means 26 is connected to an acquisition system, and the information that is provided is, for example, used by the control system of the device 1 to monitor its operation.
As
Likewise, and as illustrated in
These portions 29, for example in bellows form, thus allow increased radial or axial compliance.
So as to provide a complete integrated operating module, of small size, the device 1 can comprise a solenoid valve 27 for control of the injection of fluid, structurally coupled to one 5 of the end parts or segments that form jaws 5, 5′.
One skilled in the art understands that the device 1 according to the invention makes it possible to monitor the translational motion that is one of the basic motions of any robotic system, and at the same time produces the drive unit of this motion. The integration of two functions into one component, owing to the rigidity and the design of the device 1 in the directions other than the direction of motion, makes possible a unique compactness.
The proposed device 1 also inherently offers an axial compliance, tied to the characteristic of the central chamber 6′ that can be modified in design. This compliance is an important element for safety as disclosed above.
Additional design compliances can be integrated by particular configurations of the parts 5, 5′ and 6 as indicated above; the proposed embodiments based on polymer materials and on the excellent power-to-weight ratio of pneumatic technologies make it possible, for example, to propose a very light component for shaping low-weight robotic arms.
Finally, the device 1 forms an actuator that constitutes a safe and reliable means for monitoring motive forces by simply modulating a value that is the pressure inside the unit of the central chamber and jaws: this is in fact a particularly reliable mechanical force limiter.
The invention also relates, as
This system comprises, on the one hand, at least one pneumatic holding and moving device carried by a specific support 18′ or made integral with the patient 19 and placed in direct contact with the skin 19′ of the latter, on the other hand, at least one pressurized gaseous fluid source, and, finally, a man-machine control interface 18, optionally being part of a medical installation.
This system is characterized in that said at least one pneumatic holding and moving device consists of a device 1 as described above, with its hollow body 1′ being held at its front-end part 5.
The invention also relates to a controlled, preferably automated, system for insertion and optionally assembly or mounting, by translational motion, optionally combined with a rotational motion of an elongated object 2, such as a structural piece, tool or instrument, in a passage, an opening or a receiving housing adapted for another object, piece, part, element or the like (not shown).
This system is characterized in that it comprises at least one pneumatic device 1 for guided holding and moving as described above, with said device 1 being mounted on an optionally movable support means, such as a robot arm or a collaborative robot, with said device 1 being an integral part, if necessary, of said robot arm or robot.
For the purpose of increasing the thrust force that can be applied to the object 2, it can be provided that the system comprises at least two pneumatic holding and moving devices 1, arranged in an aligned manner according to their axial direction DA (i.e., the axial directions DA of the devices 1 are combined) and each traversed by the elongated object 2 to hold and move automatically on command, with said devices 1 being fed with pressurized fluid in a coordinated manner (not shown).
By way of example,
Finally, the object of the invention is also a method for inserting an elongated instrument or tool into the body of a subject by means of a system that is mentioned above.
This method is characterized in that it consists in installing at least one pneumatic holding and moving device 1 by aligning its axial direction DA with an inlet opening made in advance in the skin 19′ of the subject 19, then installing the instrument or the tool in the axial passage 4 of the hollow body 1′ of the device 1 up to a predetermined insertion position, then gradually and sequentially depressing said tool or instrument 2 by carrying out successively, for each elementary step of movement, a pressurized fluid injection phase and a phase for evacuating said fluid, with the injection phase being interrupted when the rear terminal chamber 7′ of the multi-chamber hollow body 1′ has reached an internal pressure that corresponds to its operational pressure, and repeating the cycle of the two above-mentioned phases as many times as necessary to reach the translational movement amplitude, and even the degree of depression, that is desired.
Finally, the invention also relates to a method for inserting an elongated object 2, such as a structural piece, tool or instrument, into an opening or a passage of a piece by means of the above-mentioned controlled system.
This method is characterized in that it consists in installing at least one pneumatic holding and moving device 1 by aligning its axial direction DA with the inlet opening of the opening or the passage in question, with the elongated object 2 being in place in the axial passage 4 of the hollow body 1′ of the device 1, then gradually and sequentially depressing said object 2 by successively carrying out, for each elementary step of movement, a pressurized fluid injection phase and a phase for evacuating said fluid, with the injection phase being interrupted when the rear terminal chamber 5′ of the multi-chamber hollow body 1′ has reached an internal pressure that corresponds to its operational pressure, and repeating the cycle of the two above-mentioned phases as many times as necessary to reach the amplitude of the translational movement, and even the degree of depression, that is desired.
When a continuous engagement of the device on the object 2 throughout the depression motion is desired, it may be provided that the injection phase of the next cycle begins while the evacuation phase of the cycle currently under way has yet to be completed (see
The difference between the kinematics of
Of course, the invention is not limited to the embodiments described and shown in the accompanying drawings. Modifications can still be made, in particular from the standpoint of the composition of the various elements or by substitution of technical equivalents, without thereby exceeding the scope of protection of the invention.
Number | Date | Country | Kind |
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1561373 | Nov 2015 | FR | national |
Filing Document | Filing Date | Country | Kind |
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PCT/FR2016/053078 | 11/24/2016 | WO | 00 |