W 0001/02 (Non-unity "a posteriori" (no)) 20-08-2002

Reasons for the Decision

1. The protest is admissible.

2. Rule 68.3 c) PCT states that an applicant may pay an additional search fee under protest, that is, accompanied by a reasoned statement to the effect that the international application complies with the requirement of unity of invention or that the amount of the required additional examination fee is excessive.

3. In the present case, the applicant paid examination fees for the inventions A, B, D and E identified in the invitation of the IPEA to restrict or to pay additional fees. However, as follows from the statement accompanying the protest, only one of these fees was paid under protest as the applicant only discusses the novel technical feature common to inventions A an E but gives no arguments as to inventions B and D. The Board therefore needs only to consider the question of whether the IPEA's reasoning with respect to inventions A and E is sufficient to substantiate a finding of lack of unity.

4. In its invitation referred to above the IPEA argued that document D1 (US-A-5072733) completely anticipated the sensor assembly set out in claim 1 ("invention A"). It is thus apparent that the IPEA's objection is an "a posteriori" objection made after taking prior art document D1 into consideration. Thus, it has to be examined first whether the first group of inventions ("invention A") was anticipated by this prior art.

5.1. Document D1 is concerned with a shock wave lithotripter designed to fragment urinary tract stones, gall stones, renal and ureteral stones. For calibrating and focussing the lithotripter, ultrasound imaging is employed to locate the stone to be fragmented. To this end, a conventional ultrasound probe (for example a sector scan probe) having a transducer for producing ultrasound beams defining a plane of radiation during calibration of the lithotripter is used (cf. D1, column 2, lines 38 to 52; column 3, lines 7 to 12). The ultrasound probe is associated with a display apparatus comprising a screen on which the echoes produced at the interfaces between different tissue in the plane illuminated by the ultrasonic beams in the patient can be identified as differences in brightness (cf. D1, column 5, lines 6 to 15; Figure 3B).

5.2. Compared with the medical sensor assembly stipulated in claim 1 of the application, document D1 does not explicitly mention a "storage device operatively connected to the transducer to store data which are retrievable from the storage device subsequent to being stored". It may be argued - as has been done by the IPEA - that for generating a sector image or for operating the transducer, a storage device adapted to store data related to the transducer is always necessary and, therefore, implicitly provided in the ultrasound sector scanning assembly disclosed in D1 so that the medical sensor according to claim 1 lacks novelty vis-à-vis the conventional ultrasound probe given in D1. In the Board's view it nevertheless remains doubtful whether the storage device according to claim 1 of the application and the device implicitly disclosed in document D1 are in fact in all technical details the same.

6.1. It follows from Rule 13.2 PCT, setting out the circumstances in which the requirement of unity of invention shall be fulfilled, that a group of inventions (in the present case inventions A and E defined by claims of the same category) claimed in the same international application is only linked so as to form a single general inventive concept within the terms of Rule 13.1 PCT when there is a technical relationship among those inventions involving one or more of the same or corresponding special technical features. Given that these special technical features shall define the contribution which each of the claimed inventions, considered as a whole, makes over the prior art, either a common structural feature or a common functional technical feature must be present which does not yet belong to or is not rendered obvious by the state of the art (see W 0004/96, point 7).

6.2. As to "invention A", the claimed medical sensor assembly is, however, not restricted to the technical features given in independent claim 1 but comprises further embodiments given in five dependent claims. After the possible demise of independent claim 1 on account of the subject-matter's lack of novelty, the question, therefore, arises whether the subject matter of the remaining claims 2 to 6 and any new independent claim formed by combining claim 1 with a dependent claim are still so linked as to form a single general inventive concept. As can be noted, any of dependent claims 2 to 6 is directed to a medical sensor assembly comprising a transducer element which allows to determine the blood pressure. Hence, in the Board's view, the dependent claims 2 to 6 are so linked as to form a single general concept which is not disclosed in document D1 and therefore novel. In the absence of any evidence to the contrary, the Board has no reason to conclude that this concept would not be "inventive", either.

6.3. Likewise, the apparatus according to claims 27 to 31 of "invention E" is designed for measuring the blood pressure. It includes first and second transducer elements, first and second storage devices whereby at least the second transducer element and the second storage device are removable, and a processor. Moreover, the second transducer element in "invention E" is selected to be a "pressure transducer" which corresponds to the embodiment claimed in claims 2 to 6 of "invention A". Although the apparatus claimed in "invention E" has to be regarded as being more sophisticated than the sensor assembly claimed in "invention A", both inventions nevertheless include the same "special technical features" which aim at solving the same technical problem. This problem is, however, neither addressed in D1 and also appears to be different from that underlying the conventional ultrasound probe disclosed in document D1 which is directed to ultrasound imaging.

7. If, as in the present case, the search revealed prior art more relevant than that already acknowledged in the description of the international patent application (in the present case: document D1), it is indispensable for determining unity of invention to define, on the basis of the disclosure of this prior art (here document D1), the technical problem(s) to be solved by the different invention(s). Thus, unity of invention can be assessed only after having determined the technical problem in such a manner (see W 0006/97, points 6.2 to 6.4).

8. In the present case, however, neither the annex to the IPEA's invitation to restrict or to pay additional fees of 27 July 2001 nor the finding of the review panel of 17. October 2001 comprised a detailed analysis of the technical problem(s) underlying the identified inventions A and E in view of both, the disclosure of the international application and document D1 as relevant state of the art. Rather, it was objected that the features common to independent claims 1 and 27 were not novel vis-à-vis the teaching of document D1 was objected. This approach is, however, not sufficient to substantiate the objection of lack of unity between inventions A and E.

9. Given this situation, the IPEA's statement cannot be accepted as a valid argument in support of the finding of lack of unity of invention. In this situation, the Board is unable to concur with the reasoning in the IPEA's invitation to pay an additional fee for "invention E" based exclusively on its finding that claim 1 of "invention A" was anticipated by document D1. Rather it follows from the above considerations that the special technical features common to both inventions A and E are neither known nor derivable in an obvious way from the teaching given in document D1.