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England and Wales Court of Appeal (Civil Division) Decisions |
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You are here: BAILII >> Databases >> England and Wales Court of Appeal (Civil Division) Decisions >> Occlutech GmbH v AGA Medical Corporation [2010] EWCA Civ 702 (22 June 2010) URL: http://www.bailii.org/ew/cases/EWCA/Civ/2010/702.html Cite as: [2010] EWCA Civ 702 |
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ON APPEAL FROM THE HIGH COURT, CHANCERY DIVISION,
PATENTS COURT
MANN J
HC07C02048
Strand, London, WC2A 2LL |
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B e f o r e :
LORD JUSTICE PATTEN
and
SIR PAUL KENNEDY
____________________
OCCLUTECH GmbH |
Respondent |
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- and - |
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AGA MEDICAL CORPORATION |
Appellant |
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- and - |
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DOT MEDICAL LIMITED |
Third Party |
____________________
Peter Prescott QC (instructed by Marks&Clerk Solicitors LLP) for the Respondent
Hearing dates : 25th and 26th May 2010
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Crown Copyright ©
Lord Justice Patten :
Introduction
"1. A collapsible medical device (60) comprising a metal fabric formed of braided metal strands, the device (60) having a collapsed configuration for delivery through a channel in a patient's, and has a generally dumbbell-shaped expanded configuration with two expanded diameter portions (64) separated by a reduced diameter portion (62) formed between opposed ends of the device, characterized in that clamps (15) are adapted to clamp the strands at the opposed ends of the device.
16. A method of forming a medical device according to any one of the preceding claims, the method comprising the steps of:
(a) providing a metal fabric formed of a plurality of braided strands, the strands being formed of a metal which can be heat treated to substantially set a desired shape;
(b) deforming the metal fabric to generally conform to an internal wall surface of a moulding element:
(c) heat treating the metal fabric in contact with the surface of the moulding element at an elevated temperature, the temperature and the duration of the heat treatment being sufficient to substantially set the shape of the fabric in its deformed state;
(d) removing the metal fabric from contact with the moulding element; and
(e) clamping the opposite end."
"[0001] The present invention generally relates to intravascular devices for treating certain medical conditions. The devices in accordance with the invention are particularly well suited for delivery through a catheter or the like to a remote location in a patient's vascular system or in analogous vessels within a patient's body.
[0002] A wide variety of intravascular devices are used in various medical procedures. Certain intravascular devices, such as catheters and guidewires, are generally used simply to deliver fluids or other medical devices to specific locations within a patient's body, such as a selective site within the vascular system. Other, frequently more complex, devices are used in treating specific conditions, such as devices used in removing vascular occlusions or for treating septa1 defects and the like.
[0003] In certain circumstances, it may be necessary to occlude a patient's vessel, such as to stop blood flow through an artery to a tumour or other lesion. Presently, this is commonly accomplished simply by inserting, e.g. Ivalon particles, a trade name for vascular occlusion particles, and short sections of coil springs into a vessel at a desired location. These "embolisation agents" will eventually become lodged in the vessel, frequently floating downstream of the site at which they are released before blocking the vessel. In part due to the inability to precisely position the embolisation agents, this procedure is often limited in its utility."
"[0007] Accordingly, it would be advantageous to provide a reliable embolisation device which is both easy to deploy and can be accurately placed in a vessel.
[0008] According to the present invention, a collapsible medical device comprises a metal fabric formed of braided metal strands, the device having a collapsed configuration for delivery through a channel in a patient's body and a generally dumbbell-shaped expanded configuration with two expanded diameter portions separated by a reduced diameter portion formed between the opposed ends of the device, and clamps for clamping the strands of the opposed ends of the device.
[0009] A collapsible medical device having a dumpbell-shaped expanded configuration is disclosed in the international application WO-A-94112136."
"[0010] Such devices of the invention are formed of a metal fabric and have an expanded configuration and a collapsed configuration. The devices are collapsed for deployment through a catheter and, upon exiting the distal end of the catheter in a patient's channel, will resiliently substantially return to their expanded configuration.
[0011] The device of the present invention can be formed from a metal fabric formed of a plurality of resilient strands, with the wires being formed of a resilient material which can be heat-treated to substantially set a desired shape. The fabric is then deformed to generally conform to a moulding surface of a moulding element, and the fabric is heat-treated in contact with the surface of the moulding element at an elevated temperature….after the heat treatment, the fabric is removed from contact with the moulding element and will substantially retain its shape in the deformed state. The fabric so treated defines an expanded state of a medical device which can be deployed through a catheter into a channel in a patient's body.
[0012] The present invention will be described, by way of example, with reference to the accompanying drawings, in which:
Figures 1A and 1B depict a metal fabric suitable for use with the invention;
…
Figures 5A and 5B are a side view and an end view, respectively, of a medical device in accordance with the invention."
"[0013] The present invention provides a device and discloses a reproducible, relatively inexpensive method of forming devices for use in channels in patients' bodies, such as vascular channels, urinary tracts, biliary ducts and the like, as well as devices which may be made via that method. In forming a medical device, a metal fabric 10 is provided. The fabric is formed of a plurality of wire strands having a predetermined relative orientation between the strands. Figures 1 A and 1 B illustrate two examples of metal fabrics which are suitable for use.
[0014] In the fabric of Figure 1 A, the metal strands define two sets of essentially parallel generally helical strands, with the strands of one set having a "hand", i.e. a direction of rotation, opposite that of the other set. This defines a generally tubular fabric, known in the fabric industry as a tubular braid….
[0018] Figure 1B illustrates another type of fabric which is suitable for use. This fabric is a more conventional fabric and may take the form of a flat woven sheet, knitted sheet or the like. In the woven fabric shown in Figure 1 B, there are also two sets 14 and 14' of generally parallel strands, with one set of strands being oriented at an angle, e.g. generally perpendicular (having a pick of about 90°), with respect to the other set. As noted above, the pitch and pick of this fabric (or, in the case of a knit fabric, the pick and the pattern of the kit, e.g. Jersey or double knits) may be selected to optimise the desired properties of the final medical device.
[0019] The wire strands of the metal fabric should be formed of a material which is both resilient and can be heat treated to substantially set a desired shape….
[0020] One class of materials which meet these qualifications are so-called shape memory alloys. Such alloys tend to have a temperature induced phase change which will cause the material to have a preferred configuration which can be fixed by heating the material above a certain transition temperature to induce a change in the phase of the material. When the alloy is cooled back down, the alloy will "remember" the shape it was in during the heat treatment and will tend to assume that configuration unless constrained from so doing.
[0021] One particularly preferred shape memory alloy for use in the present invention is nitinol, an approximately stoichiometric alloy of nickel and titanium, which may also include other minor amounts of other metals to achieve desired properties.
……
[0023] In preparation of forming a medical device in keeping with the invention, an appropriately sized piece of the metal fabric is cut from the larger piece of fabric which is formed, for example, by braiding wire strands to form a long tubular braid. The dimensions of the piece of fabric to be cut will depend, in large part, upon the size and shape of the medical device to be formed therefrom.
[0024] When cutting the fabric to the desired dimensions, care should be taken to ensure that the fabric will not unravel. In the case of tubular braids formed of NiTi alloys, for example, the individual wire strands will tend to return to their heat-set configuration unless constrained. If the braid is heat treated to set the strands in the braided configuration, they will tend to remain in the braided form and only the ends will become frayed. However, it may be more economical to simply form the braid without heat treating the braid since the fabric will be heat treated again in forming the medical device, as noted below.
[0025] In such untreated NiTi fabrics, the strands will tend to return to their unbraided configuration and the braid can unravel fairly quickly unless the ends of the length of braid cut to form the device are constrained relative to one another. One method which has proven to be useful to prevent the braid from unravelling is to clamp the braid at two locations and cut the braid to leave a length of the braid having clamps (15 in Figure 2) at either end, thereby effectively defining an empty space within a sealed length of fabric. These clamps 15 will hold the ends of the cut braid together and prevent the braid from unravelling.
[0026] Alternatively, one can solder, braze, weld or otherwise affix the ends of the desired length together (e.g. with a biocompatible cementitious organic material) before cutting the braid. Although soldering and brazing of NiTi alloys has proven to be fairly difficult, the ends can be welded together, such as by spot welding with a laser welder."
"[0027] The same problems present themselves when a flat sheet of fabric such as the woven fabric shown in Figure 1 B is used. With such a fabric, the fabric can be inverted upon itself to form a recess or depression and the fabric can be clamped about this recess to form an empty pocket (not shown) before the fabric is cut. If it is desired to keep the fabric in a generally flat configuration, it may be necessary to weld the junctions of the strands together adjacent the periphery of the desired piece of fabric before that piece is cut from the larger sheet. So connecting the ends of the strands together will prevent fabrics formed of untreated shape memory alloys and the like from unravelling during the forming process."
"[0041] As noted above, the ends of the tubular braid should be secured in order to prevent the braid from unraveling. Each end of the metal fabric 10 is desirably received within a cavity 46 formed in one of the two end plates 40. If a clamp (15 in Figure 2) is used, the clamp may be sized to be relatively snugly received within one of these cavities 46 in order to effectively attach the end of the fabric to the end plate 40…."
"The clamp may serve to connect the device to a delivery system (not shown). In this case, the clamp may be generally cylindrical in shape and have a recess for receiving the ends of the wires to substantially prevent the wires from moving relative to one another, and a threaded outer surface. The threaded outer surface is adapted to be received within a cylindrical recess (not shown) on a distal end of a delivery device and to engage the threaded inner surface of the delivery device's recess."
"[0071] While a preferred embodiment of the present invention has been described, it should be understood that various changes, adaptations and modifications may be made therein without departing from the invention and the scope of the appended claims."
"8. The products in respect of which declarations of non-infringement are sought are described in a process and product description and the same description can be taken as applying to all the allegedly infringing products if different from those which are the subject of the declaration. The old and new are essentially the same apart from the method of fixing the loose strands of the devices. The common elements are as follows:
i) A braided fabric formed from monofilament nitinol wires is used.
ii) It is formed into a sock. The distal end (farthest from the open end of the catheter) is closed; the proximal end is open and terminates in some loose wires which are not braided, or not braided to the extent that they form a fabric.
iii) The sock is placed into a mould conforming to the shape of the final intended product. The end with the ends of the strands protrudes through a hole at one end of mould.
iv) The mould is then heated to a temperature sufficient to make the nitinol keep its desired shape. That shape in the picture is of two saucer like disks, one slightly smaller than each other, separated by a wider mid-piece, though the actual products that I have seen do not reflect that difference in shape. Nothing turns on that.
v) The newly shaped product is then removed from the mould.
9. At this point the old and new products depart. The next stage, according to the description, is the fixing of the loose ends of the device - what was formerly the open end of the sock. According to the description, but as supplemented by further oral evidence, the following steps take place in relation to the old Occlutech device.
i) A copper wire is wound around the loose ends of the strands at their ends to gather them together for the next phase.
ii) Then a nitinol sleeve in the form of a hollow cylinder and having an internal diameter slightly larger than the diameter of the bundle of nitinol wires is slid up the gathered wires and the assembly inverted to stop the sleeve falling off. Then the copper wire is removed. The wire is sufficiently loose to be able to be slipped off.
iii) The protruding wires are cut flush with the proximal end of the sleeve, by a laser beam. The assembly is retained in the inverted position.
iv) The bundle of wires is then subjected to microplasma welding to fuse the wires together and to the nitinol sleeve. "The ends of wires have been merged together with each other and with the proximal end of the sleeve to form a welded clot of nitinol."
v) An adaptor "for delivery purposes" may then be fitted. It is cylindrical and its distal end is of a size to mate with the nitinol clot; the proximal bore is internally threaded. It is pushed over the clot of nitinol and spot welds applied by laser beam to deform inwardly the inner and outer walls of the adaptor. The adapter has an internal thread at its proximal end for fixing it on to the delivery wire.
10. It should be noted from this description that only one end of the device is subjected to this welding and sleeving process. The other end is the former closed end of the sock - the fibres pass continuously around it.
11. For the new device the sock and moulding processes are essentially the same. The differences come after the moulding process.
12. At this point the device is put in a template which has a hole through which the loose ends of the device protrude. Then the following steps take place:
i) The loose ends are cut almost, but not quite, flush with the face of the template, by using a laser beam. Short lengths are left protruding.
ii) The loose ends are subjected to microplasma arc welding to fuse the wires to each other. They form a welded nitinol clot.
iii) At that point the device is in its final configuration save for the addition of an adaptor for delivery purposes.
iv) As with the old devices, the adaptor is a sleeve which fits over the clot and is threaded at the proximal end. It is pushed over the clot and weld spots are applied radially by means of a laser beam. This deforms the inner and outer walls of the adaptor.
13. Accordingly, as with the old devices, the welding and other operations go on at one end of the device only. The other end is still the closed end of the sock, formed by the fibres passing round and returning to the originally "open" end."
(i) Are the Occlutech devices clamped in the sense described in claims 1 and 16 of the patent, given that the ends of the metal strands are secured together by welding?;
(ii) What do the words "clamps (15) are adapted to clamp the strands at the opposed ends of the device" in claim 1 mean? Are the Occlutech devices clamped in this way, given that the metal fibres all terminate at one end of the device rather than at both ends?; and
(iii) Are the Occlutech devices "dumbbell-shaped" as described in the patent specification?
"[182] The task for the court is to determine what the person skilled in the art would have understood the patentee to have been using the language of the claim to mean. The principles were summarised by Jacob LJ in Mayne Pharma v Pharmacia Italia [2005] EWCA Civ 137 and refined by Pumfrey J in Halliburton v Smith International [2005] EWHC 1623 (Pat) following their general approval by the House of Lords in Kirin-Amgen v Hoechst Marion Roussel [2005] RPC 9. An abbreviated version of them is as follows:
(i) The first overarching principle is that contained in Article 69 of the European Patent Convention;
(ii) Article 69 says that the extent of protection is determined by the claims. It goes on to say that the description and drawings shall be used to interpret the claims. In short the claims are to be construed in context.
(iii) It follows that the claims are to be construed purposively—the inventor's purpose being ascertained from the description and drawings.
(iv) It further follows that the claims must not be construed as if they stood alone—the drawings and description only being used to resolve any ambiguity. Purpose is vital to the construction of claims.
(v) When ascertaining the inventor's purpose, it must be remembered that he may have several purposes depending on the level of generality of his invention. Typically, for instance, an inventor may have one, generally more than one, specific embodiment as well as a generalised concept. But there is no presumption that the patentee necessarily intended the widest possible meaning consistent with his purpose be given to the words that he used: purpose and meaning are different.
(vi) Thus purpose is not the be-all and end-all. One is still at the end of the day concerned with the meaning of the language used. Hence the other extreme of the Protocol—a mere guideline—is also ruled out by Article 69 itself. It is the terms of the claims which delineate the patentee's territory.
(vii) It follows that if the patentee has included what is obviously a deliberate limitation in his claims, it must have a meaning. One cannot disregard obviously intentional elements.
(vii) It also follows that where a patentee has used a word or phrase which, acontextually, might have a particular meaning (narrow or wide) it does not necessarily have that meaning in context.
(vii) It further follows that there is no general "doctrine of equivalents."
(viii) On the other hand purposive construction can lead to the conclusion that a technically trivial or minor difference between an element of a claim and the corresponding element of the alleged infringement nonetheless falls within the meaning of the element when read purposively. This is not because there is a doctrine of equivalents: it is because that is the fair way to read the claim in context.
(ix) Finally purposive construction leads one to eschew the kind of meticulous verbal analysis which lawyers are too often tempted by their training to indulge."
"33. In the case of a patent specification, the notional addressee is the person skilled in the art. He (or, I say once and for all, she) comes to a reading of the specification with common general knowledge of the art. And he reads the specification on the assumption that its purpose is to both to describe and to demarcate an invention - a practical idea which the patentee has had for a new product or process - and not to be a textbook in mathematics or chemistry or a shopping list of chemicals or hardware. It is this insight which lies at the heart of "purposive construction". If Lord Diplock did not invent the expression, he certainly gave it wide currency in the law. But there is, I think, a tendency to regard it as a vague description of some kind of divination which mysteriously penetrates beneath the language of the specification. Lord Diplock was in my opinion being much more specific and his intention was to point out that a person may be taken to mean something different when he uses words for one purpose from what he would be taken to mean if he was using them for another. The example in the Catnic case was the difference between what a person would reasonably be taken to mean by using the word "vertical" in a mathematical theorem and by using it in a claimed definition of a lintel for use in the building trade. The only point on which I would question the otherwise admirable summary of the law on infringement in the judgment of Jacob LJ in Rockwater Ltd v Technip France SA (unreported) [2004] EWCA Civ 381, at paragraph 41, is when he says in sub-paragraph (e) that to be "fair to the patentee" one must use "the widest purpose consistent with his teaching". This, as it seems to me, is to confuse the purpose of the utterance with what it would be understood to mean. The purpose of a patent specification, as I have said, is no more nor less than to communicate the idea of an invention. An appreciation of that purpose is part of the material which one uses to ascertain the meaning. But purpose and meaning are different. If, when speaking of the widest purpose, Jacob LJ meant the widest meaning, I would respectfully disagree. There is no presumption about the width of the claims. A patent may, for one reason or another, claim less than it teaches or enables.
34. "Purposive construction" does not mean that one is extending or going beyond the definition of the technical matter for which the patentee seeks protection in the claims. The question is always what the person skilled in the art would have understood the patentee to be using the language of the claim to mean. And for this purpose, the language he has chosen is usually of critical importance. The conventions of word meaning and syntax enable us to express our meanings with great accuracy and subtlety and the skilled man will ordinarily assume that the patentee has chosen his language accordingly. As a number of judges have pointed out, the specification is a unilateral document in words of the patentee's own choosing. Furthermore, the words will usually have been chosen upon skilled advice. The specification is not a document inter rusticos for which broad allowances must be made. On the other hand, it must be recognised that the patentee is trying to describe something which, at any rate in his opinion, is new; which has not existed before and of which there may be no generally accepted definition. There will be occasions upon which it will be obvious to the skilled man that the patentee must in some respect have departed from conventional use of language or included in his description of the invention some element which he did not mean to be essential. But one would not expect that to happen very often.
35 One of the reasons why it will be unusual for the notional skilled man to conclude, after construing the claim purposively in the context of the specification and drawings, that the patentee must nevertheless have meant something different from what he appears to have meant, is that there are necessarily gaps in our knowledge of the background which led him to express himself in that particular way. The courts of the United Kingdom, the Netherlands and Germany certainly discourage, if they do not actually prohibit, use of the patent office file in aid of construction. There are good reasons: the meaning of the patent should not change according to whether or not the person skilled in the art has access to the file and in any case life is too short for the limited assistance which it can provide. It is however frequently impossible to know without access, not merely to the file but to the private thoughts of the patentee and his advisors as well, what the reason was for some apparently inexplicable limitation in the extent of the monopoly claimed. One possible explanation is that it does not represent what the patentee really meant to say. But another is that he did mean it, for reasons of his own; such as wanting to avoid arguments with the examiners over enablement or prior art and have his patent granted as soon as possible. This feature of the practical life of a patent agent reduces the scope for a conclusion that the patentee could not have meant what the words appear to be saying. It has been suggested that in the absence of any explanation for a restriction in the extent of protection claimed, it should be presumed that there was some good reason between the patentee and the patent office. I do not think that it is sensible to have presumptions about what people must be taken to have meant but a conclusion that they have departed from conventional usage obviously needs some rational basis."
"The German approach to the question of equivalents can be summarized as follows:
The main basis for the determination of the scope of patent protection is the patent claim and an understanding by a person skilled in the art of the technical teaching embodied in such a claim. For this purpose, a patent claim has to be interpreted in conjunction with both the description of the invention and the drawings. In doing so, the basic principles of function-aimed interpretation of the terms used in the patent claim, as well as a context-based interpretation, are to be followed. A contested embodiment which falls within the meaning of the claim so construed infringes the patent literally.
A patent can also be infringed if the contested embodiment does not fall within the "literal" scope of the patent claim. This extension in the scope of the patent is to bring about an adequate level of protection of the inventive achievement in a way that also ensures the highest possible level of legal certainty. This optimal balance is achieved by protecting only those variants that the patent claim (and not just the prior art) has made obvious to a person skilled in the art, on the priority date. That is the case, if the following questions 1 to 3 are answered in the affirmative and, in addition, question 4 is answered in the negative:
1. Does the modified embodiment solve the problem underlying the invention by means which have objectively the same technical effect?
2. Was the person skilled in the art enabled by her specialist knowledge on the priority date to find that the modified means would have the same effect?
3. While answering question 2, are the considerations that the person skilled in the art applies drawn from the technical teaching of the patent claim (so that the person skilled in the art took the modified embodiment into account as being an equivalent solution)?
4. Is the modified embodiment anticipated or made obvious by the state of the art?"
"(3) Would the reader skilled in the art nevertheless have understood from the language of the claim that the patentee intended that strict compliance with the primary meaning was an essential requirement of the invention? If yes, the variant is outside the claim."
"40. There seems to be no clear English authority on the point, even at first instance. In Bristol-Myers Squibb Co v Baker Norton Inc [1999] RPC 253, 274-5 Jacob J has given a useful summary of the problems associated with taking account of what he called prosecution history – that is, the vicissitudes of an application file's progress through the official system – as an aid to construction of the final specification. But Jacob J said that he did not have to decide anything about the point.
41. This court was shown a decision of the Supreme Court of the Netherlands, Ciba-Geigy v Oté Optics (13 January 1995) which contains a helpful statement of principle. In explaining that the Court of Appeal had gone too far in excluding all reference to the file, the Supreme Court said:
"Article 69, paragraph 1 of the EPC as interpreted in accordance with the protocol relating thereto does indeed purport (among other things) to ensure reasonable certainty for third parties, but it does not follow that the information from the granting file that is available to third parties may never be used in support of the interpretation given by the patentee to his patent. The requirement of reasonable certainty for third parties does, however, call for restraint in using arguments derived from the granting file in favour of the patentee. Consequently, a court will only be justified in using clarifying information from the public part of the granting file, when it holds that even after the average person skilled in the art has considered the description and the drawings, it is still open to question how the contents of the claims must be interpreted. In this connection one must also take into consideration that the risk of any ambiguities due to careless wording of the patent specification must in principle lie with the patentee."
42. Apart from the last sentence (which raises a different point, and on which Mr Floyd did not rely) I would treat this as persuasive guidance. The letter to the European Patent Office did not have the same status as published prior art identified in a specification, which is readily admissible. But it did contain objective information about and commentary on experiments which were conducted in response to official observations, and it could be of assistance in resolving some puzzling features of the specification. Although the prosecution process may sometimes superficially resemble a process of negotiation between the applicant and its advisers and the officials who scrutinise the file, it is not the sort of commercial negotiation which is still rigidly excluded in the construction of a written contract (see Investors Compensation Scheme v West Bromwich Building Society [1998] 1 WLR 896, 913). Had it been necessary for the judge to take account of the letter in order to resolve the issue of construction, I consider that he would have been entitled to do so."
"Clamps"
"A device (as a band or brace) designed to bind or constrict two or more parts together so as to hold them firmly in their relative position."
"A brace, clasp, or band, usually of iron or other rigid material, used for giving strength or support to flexible or moveable objects, or for fastening two or more things securely together".
"Something held together by soldering, welding, gluing or similar mechanisms would not naturally, or at least not immediately, fall within that meaning. However, one has to consider whether the patent has an extended meaning going beyond physical compression by a particular object. In my view it is plain that, on the wording of the patent, it does not. This is apparent from the following:
i) There is a small indication from the words in claim 1 itself - "clamps are adapted to clamp the strands". The repetition tends to suggest that the word is used in its normal sense. By itself, however, this is not strong.
ii) The point begins to look stronger because the claim contains a cross-reference to figure 5 A via the numerical reference to "(15)". That figure appears in Appendix 2 to this judgment. It shows something which is fairly clearly representative of a clamp.
iii) The more one reads the description and the embodiments the clearer this view becomes. This is particularly apparent from paragraphs 0025 and 0026, set out above. Paragraph 0025 refers to "clamps (15 in figure 2 [should be 5A]) … [which] will hold the ends of the cut braid together …".
iv) This is put pretty much beyond doubt by paragraph 0026 which in terms distinguishes other techniques, - "Alternatively, one can solder, braze, weld or otherwise affix the ends …". Thus clamping is said not to indicate these alternative methods of fixing.
v) Other references to clamps support this. Thus paragraph 41 suggests how a clamp can be sized. It is hard to see how this can refer to anything other than a clamp in the ordinary sense of the word, which excludes such things as soldering or welding."
"Mr Howe's argument sought to turn these textual references on their head. He said that soldering, brazing and so on were taught in paragraph 0026 as "alternative methods of achieving [the objective of preventing unravelling] to clamping. Thus, this is a case where the Patentee has made a 'dictionary definition of his specification' and the word 'clamp' in the claims is to be construed as embracing these alternative disclosed methods of securing the ends of the strands." I am afraid I do not follow this reasoning. The juxtaposition of paragraphs 0025 and 0026 demonstrate that the patentee has not provided a sort of dictionary definition of "clamp". He has referred to clamps, and then referred to alternatives to clamps. I do not understand how this amounts to defining clamps to include those other "not clamps" (as it were). "
Clamping the stands at the opposed ends of the device
"… One must agree with the defendants that claims 1 and 16 of the patent in suit, seen from a philological point of view, teach several clamps (plural) and in addition to that prescribe that these clamps are adapted to clamp the strands at opposed ends of the device. This describes configurations in which one clamp each is present at the proximal and at the opposed – distal – end. Yet the average skilled person will not content himself with this mere linguistic understanding. He will understand that the ends of the strands are supposed to be bundled with the help of the clamps, which is why feature 2e) of claim 16 – as the plaintiff rightly pointed out in the oral hearing before the present Court – refers to a clamping of the opposed ends of the strands, and not of the device, regardless of whether the strands are left lying flat or if their ends are placed on top of each other by folding, because just by taking this measure, the two ends of the strands do not cease to exist. Since the method described therein is supposed to result in a device of the type inter alia protected by claim 1, the skilled person will assume that the technical meaning of claim 1 also includes embodiments in which both strand ends are placed on top of each other and are bundled at one end of the device only.
…
In the embodiment according to para. [0027], it only makes sense technically, in view of the function of the clamping which is to prevent the strand ends from unravelling, to provide clamps where free strand ends are present. Since this is only the case on one side of the device, and all strand ends can be grasped at once with one – single – clamp, only one and not several clamps are required. The plural "clamps" used in the claim does not stand in the way of this view. The skilled person does not glean from the wording that several clamps should be used in any case; in view of the embodiment described in para [0027], he will understand the term "clamps" as a generic term which specifies which type of device – i.e. clamps – is supposed to be used in order to prevent the strand ends from fraying…."
Conclusion
Sir Paul Kennedy :
Lord Justice Pill :
1. Patent in suit
2. Occlutech PPD
3. Boston Scientific