ZOMEDICA Come full circle. | Decision 2719998

OPPOSITION DIVISION
OPPOSITION No B 2 719 998
Z-Medica, LLC, 4 Fairfield Blvd., Wallingford Connecticut 06492, United States of
America (opponent), represented by Arnold & Siedsma, A.J. Ernststraat 595F, 1082
LD Amsterdam, The Netherlands (professional representative)
a g a i n s t
Zomedica Pharmaceuticals Inc., 3928 Varsity Drive, Ann Arbor Michigan 48108,
United States of America (applicant), represented by Lane IP Limited, 2
Throgmorton Avenue, London EC2N 2DG, United Kingdom (professional
representative).
On 13/10/2017, the Opposition Division takes the following
DECISION:
1. Opposition No B 2 719 998 is partially upheld, namely for the following
contested goods and services:
Class 5: Pharmaceutical preparations for animal use in the nature of
medications to treat or prevent diseases and infections, namely,
anti-parasitic drugs, anti-inflammatory medications, anesthetics,
pain medications, anti-infectives, antibiotics, and medications to
treat appetite disorders, allergies, anemia, behavioral disorders,
bone and joint diseases and disorders, cachexia, cancer,
cardiovascular disease, eye diseases and conditions, dental
diseases including tooth decay, gingivitis; Pharmaceutical
preparations for animal use in the nature of medications to treat or
prevent diseases and infections, namely, anti-parasitic drugs, anti-
inflammatory medications, anesthetics, pain medications, anti-
infectives, antibiotics, and medications to treat halitosis and
periodontal disease, diabetes, epilepsy, fungal diseases,
gastrointestinal diseases and disorders, hormonal disorders,
immune system disorders, inappetence, infectious diseases, kidney
diseases, metabolic conditions; Pharmaceutical preparations for
animal use in the nature of medications to treat or prevent diseases
and infections, namely, anti-parasitic drugs, anti-inflammatory
medications, anesthetics, pain medications, anti-infectives,
antibiotics, and medications to treat musculoskeletal disorders,
obesity, pancreatitis, pain, respiratory and infectious diseases and
disorders, reproductive disorders, skin and tissue repair, urological,
urogenital and urinary disorders, and diseases associated with
aging in animals; Pharmaceutical preparations for animal skincare,
skin disorders, surgical incisions, wounds, bites, abscesses,
infections and post-surgery infections, and severe dermatological
conditions; Pharmaceutical preparations and substances for
veterinary use, namely, vaccines; Pharmaceutical preparations for
animal use, namely, hormones; Antiviral agents for medical or
veterinary use; Ophthalmic products for animal use, namely,
ophthalmic preparations, ophthalmic solutions, ophthalmic

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suspensions, ophthalmic ointments for medical or veterinary use,
and eye drops; Dietary supplements for animals; Sanitary sterilizing
preparations; Diagnostic kits for veterinary use consisting of
reagents for use in disease testing; Protein arrays for diagnosing
cancer in animals; radiopharmaceutical imaging and detection
agents for diagnosing and monitoring cancer in animals;
Pharmaceutical and veterinary preparations for diagnosis of herpes
in cats, for treatment of canine parvo, feline aids, feline calici, feline
herpes, feline immunodeficiency diseases, and feline ocular
disease.
Class 10: Medical devices for use in the delivery of pharmaceutical
preparations to animals, namely, syringes, injectors, oral spray
devices, inhalers, species-specific drug delivery systems,
anesthetic delivery apparatus, intravenous administration sets,
pumps and bags, and gastric feeding apparatus, pumps and bags.
Class 44: Providing information and advice in the field of animal
pharmaceuticals; Pharmaceutical advice.
2. European Union trade mark application No 15 064 108 is rejected for all the
above goods and services. It may proceed for the remaining services.
3. Each party bears its own costs.
REASONS:
The opponent filed an opposition against all of the goods and services of European
Union trade mark application No 15 064 108 for the figurative mark .
However, following a limitation of the extent of the opposition on 28/10/2016, at the
moment of taking this decision the opposition is directed against some of the goods
and services covered by the trade mark application, namely against all the goods and
services in Classes 5, 10, 41 and 44. The opposition is based on international trade
mark registration No 1 045 670 for the word mark ‘Z-MEDICA’, designating the
European Union. The opponent invoked Article 8(1)(b) EUTMR.
As from 01/10/2017, Regulation (EC) No 207/2009 and Regulation (EC) No 2868/95
have been repealed and replaced by Regulation (EU) 2017/1001 (codification),
Delegated Regulation (EU) 2017/1430 and Implementing Regulation (EU)
2017/1431, subject to certain transitional provisions. All the references in this
decision to the EUTMR, EUTMDR and EUTMIR shall be understood as references to
the Regulations currently in force, except where expressly indicated otherwise.
LIKELIHOOD OF CONFUSION – ARTICLE 8(1)(b) EUTMR
A likelihood of confusion exists if there is a risk that the public might believe that the
goods or services in question, under the assumption that they bear the marks in
question, come from the same undertaking or, as the case may be, from
economically linked undertakings. Whether a likelihood of confusion exists depends
on the appreciation in a global assessment of several factors, which are
interdependent. These factors include the similarity of the signs, the similarity of the

Decision on Opposition No B 2 719 998 page: 3 of 12
goods and services, the distinctiveness of the earlier mark, the distinctive and
dominant elements of the conflicting signs and the relevant public.
a) The goods and services
The goods on which the opposition is based are the following:
Class 5: Hemostatic agents used for treating wounds; wound dressings;
bandages for dressings; sponges for dressings; gauze; first aid kits.
The contested goods and services are the following:
Class 5: Pharmaceutical preparations for animal use in the nature of
medications to treat or prevent diseases and infections, namely, anti-
parasitic drugs, anti-inflammatory medications, anesthetics, pain
medications, anti-infectives, antibiotics, and medications to treat
appetite disorders, allergies, anemia, behavioral disorders, bone and
joint diseases and disorders, cachexia, cancer, cardiovascular
disease, eye diseases and conditions, dental diseases including tooth
decay, gingivitis; Pharmaceutical preparations for animal use in the
nature of medications to treat or prevent diseases and infections,
namely, anti-parasitic drugs, anti-inflammatory medications,
anesthetics, pain medications, anti-infectives, antibiotics, and
medications to treat halitosis and periodontal disease, diabetes,
epilepsy, fungal diseases, gastrointestinal diseases and disorders,
hormonal disorders, immune system disorders, inappetence,
infectious diseases, kidney diseases, metabolic conditions;
Pharmaceutical preparations for animal use in the nature of
medications to treat or prevent diseases and infections, namely, anti-
parasitic drugs, anti-inflammatory medications, anesthetics, pain
medications, anti-infectives, antibiotics, and medications to treat
musculoskeletal disorders, obesity, pancreatitis, pain, respiratory and
infectious diseases and disorders, reproductive disorders, skin and
tissue repair, urological, urogenital and urinary disorders, and
diseases associated with aging in animals; Pharmaceutical
preparations for animal skincare, skin disorders, surgical incisions,
wounds, bites, abscesses, infections and post-surgery infections, and
severe dermatological conditions; Pharmaceutical preparations and
substances for veterinary use, namely, vaccines; Pharmaceutical
preparations for animal use, namely, hormones; Antiviral agents for
medical or veterinary use; Ophthalmic products for animal use,
namely, ophthalmic preparations, ophthalmic solutions, ophthalmic
suspensions, ophthalmic ointments for medical or veterinary use, and
eye drops; Dietary supplements for animals; Sanitary sterilizing
preparations; Diagnostic kits for veterinary use consisting of reagents
for use in disease testing; Protein arrays for diagnosing cancer in
animals; radiopharmaceutical imaging and detection agents for
diagnosing and monitoring cancer in animals; Pharmaceutical and
veterinary preparations for diagnosis of herpes in cats, for treatment of
canine parvo, feline aids, feline calici, feline herpes, feline
immunodeficiency diseases, and feline ocular disease.
Class 10: Medical devices for use in the delivery of pharmaceutical preparations
to animals, namely, syringes, injectors, oral spray devices, inhalers,

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species-specific drug delivery systems, anesthetic delivery apparatus,
intravenous administration sets, pumps and bags, and gastric feeding
apparatus, pumps and bags.
Class 41: Educational services, namely, providing classes, seminars and
workshops in the field of animal pharmaceuticals, animal healthcare,
and veterinary medicine.
Class 44: Providing information and advice in the field of animal
pharmaceuticals, animal healthcare, and veterinary medicine;
Pharmaceutical advice.
As a preliminary remark, an interpretation of the wording of the list of goods and
services is required to determine the scope of protection of these goods and
services.
The term ‘namely’, used in the applicant’s list of goods and services to show the
relationship of individual goods and services with broader categories, is exclusive
and restricts the scope of protection only to the specifically listed goods and services.
The applicant argues that, even though the comparison of goods and services is
done by reference to the specifications of the parties’ marks, this does not preclude
the taking into account of external factual information, such as actual use of the
mark, and submits some extracts from the opponent’s website. Furthermore, to
support its arguments the applicant refers to previous national proceedings before
the USPTO in respect of United States trade mark No 78 699 363 ‘Z-MEDICA’.
The Opposition Division notes that the comparison of the goods and services must
be based on the wording indicated in the respective lists of goods/services. Any
actual or intended use not stipulated in the list of goods/services is not relevant for
the comparison since this comparison is part of the assessment of likelihood of
confusion in relation to the goods/services on which the opposition is based and
directed against; it is not an assessment of actual confusion or infringement
(16/06/2010, T-487/08, Kremezin, EU:T:2010:237, § 71). Therefore, the applicants
arguments must be dismissed.
The relevant factors relating to the comparison of the goods or services include, inter
alia, the nature and purpose of the goods or services, the distribution channels, the
sales outlets, the producers, the method of use and whether they are in competition
with each other or complementary to each other.
Contested goods in Class 5
The contested pharmaceutical preparations for animal surgical incisions, wounds,
bites overlap with the opponent’s hemostatic agents used for treating wounds, insofar
as both categories include pharmaceuticals with hemostatic properties for treating
incisions or (bite) wounds in animals. Therefore, they are identical.
The contested pharmaceutical preparations for animal use in the nature of
medications to treat or prevent diseases and infections, namely, medications [for]
skin and tissue repair in animals; pharmaceutical preparations for animal skincare,
skin disorders, abscesses, infections and post-surgery infections, and severe
dermatological conditions have the same purpose as the opponent’s wound
dressings; bandages for dressings. They are directed at the same public and are
available on the same distribution channels. These goods are similar.

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The contested sanitary sterilizing preparations are commonly manufactured by the
same undertakings that offer the opponent’s wound dressings; bandages for
dressings. Such goods are directed at the same public and are distributed through
the same channels. Therefore, they are similar.
The contested dietary supplements for animals are substances prepared for special
dietary requirements, with the purpose of treating or preventing disease. Bearing this
in mind, their purpose is similar, broadly speaking, to that of the opponent’s
hemostatic agents used for treating wounds (substances used to treat specific health
issues) insofar as they are used to improve a patient’s medical condition, including in
animals. The relevant public coincides (e.g. veterinaries) and the goods generally
have the same distribution channels (e.g. veterinary supplies wholesale outlets).
Therefore, these goods are considered similar to a low degree.
The rest of the contested goods in this class are a very wide range of pharmaceutical
preparations (for example anti-inflammatory medications; anaesthetics; pain
medications; antibiotics; medications to treat appetite disorders, allergies, anemia,
cancer; vaccines; hormones; ophthalmic preparations), testing preparations,
diagnostic agents and other substances (for example diagnostic kits for veterinary
use consisting of reagents for use in disease testing; radiopharmaceutical imaging
and detection agents for diagnosing and monitoring cancer in animals), all being for
medical – including veterinary – purposes.
On the other hand, the opponent’s hemostatic agents used for treating wounds are
very specific pharmaceutical products used to stop bleeding, available in various
forms, for example, as a loose, granular powder, impregnated onto a bandage, or
retained inside a porous bag. The opponent’s goods have a similar nature and
purpose with the remaining contested goods in this class, in that they are specific
chemical products the purpose of which is, broadly speaking, healing and/or curing.
They are aimed at the same public and distributed through the same channels,
ranging from pharmacies to wholesale medical supplies outlets. They originate from
the pharmaceutical industry. However, the differences in the therapeutic indications
and possibly also the different methods of use have to be taken into consideration.
In view of the above, the Opposition Division finds that there is at least a low degree
of similarity between the opponent’s hemostatic agents used for treating wounds and
the following contested goods: pharmaceutical preparations for animal use in the
nature of medications to treat or prevent diseases and infections, namely, anti-
parasitic drugs, anti-inflammatory medications, anesthetics, pain medications, anti-
infectives, antibiotics (listed three times), and medications to treat appetite disorders,
allergies, anemia, behavioral disorders, bone and joint diseases and disorders,
cachexia, cancer, cardiovascular disease, eye diseases and conditions, dental
diseases including tooth decay, gingivitis, and to treat halitosis and periodontal
disease, diabetes, epilepsy, fungal diseases, gastrointestinal diseases and disorders,
hormonal disorders, immune system disorders, inappetence, infectious diseases,
kidney diseases, metabolic conditions, as well as to treat musculoskeletal disorders,
obesity, pancreatitis, pain, respiratory and infectious diseases and disorders,
reproductive disorders, urological, urogenital and urinary disorders, and diseases
associated with aging in animals; pharmaceutical preparations and substances for
veterinary use, namely, vaccines; pharmaceutical preparations for animal use,
namely, hormones; antiviral agents for medical or veterinary use; ophthalmic
products for animal use, namely, ophthalmic preparations, ophthalmic solutions,
ophthalmic suspensions, ophthalmic ointments for medical or veterinary use, and
eye drops; diagnostic kits for veterinary use consisting of reagents for use in disease

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testing; protein arrays for diagnosing cancer in animals; radiopharmaceutical imaging
and detection agents for diagnosing and monitoring cancer in animals;
pharmaceutical and veterinary preparations for diagnosis of herpes in cats, for
treatment of canine parvo, feline aids, feline calici, feline herpes, feline
immunodeficiency diseases, and feline ocular disease.
Contested goods in Class 10
The contested medical devices for use in the delivery of pharmaceutical preparations
to animals, namely, syringes, injectors, oral spray devices, inhalers, species-specific
drug delivery systems, anesthetic delivery apparatus, intravenous administration
sets, pumps and bags, and gastric feeding apparatus, pumps and bags are directed
at the same public as the opponent’s wound dressings; bandages for dressings in
Class 5. These goods are available through the same channels. They can be seen as
complementary in the sense that materials for dressings are indispensable for
treating a patient after the administration of pharmaceutical preparations, or at least
they are used in conjunction. Therefore, these goods are similar to a low degree.
Contested services in Class 41
The contested educational services, namely, providing classes, seminars and
workshops in the field of animal pharmaceuticals, animal healthcare, and veterinary
medicine are provided by specialised, often licensed, educational institutions such as
academies, colleges etc. The opponent argues that consumers are likely to believe
the pharmaceutical manufacturer also started an education program to teach medical
professionals and students about their products and pharmaceutical products in
general. The Opposition Division notes that such educational programs rather are
advertising activities rendered for raising the professional public’s awareness of a
drug on the market and are aimed at promoting its sales. These services do not
constitute educational services that are provided to others, for a tuition fee. The
contested services have nothing relevant in common with the opponent’s
pharmaceutical products, aside from the coincidence in the subject matter. The
contested services have no relevant commonalities with the opponent’s materials for
dressings or first aid kits either, even though such goods are used as instructional
material during first aid training courses. The natures and purposes of these goods
and services are fundamentally different. They do not coincide in the usual origin or
distribution channels. They are neither complementary nor in competition. Therefore,
the contested services are dissimilar to all of the opponent’s goods.
Contested services in Class 44
The contested providing information and advice in the field of animal
pharmaceuticals; pharmaceutical advice are considered complementary to the
opponent’s hemostatic agents used for treating wounds in Class 5. Pharmacy advice,
including the provision of information, relates to informing individuals about
medication. It may be performed by a doctor or nurse or by a pharmacist. These
goods and service coincide in the distribution channels and relevant public.
Therefore, they are similar to a low degree.
However, the same findings do not apply to the remaining contested services,
namely providing information and advice in the field of animal healthcare, and
veterinary medicine, since they are quite distinct from the provision of pharmaceutical
information. Pharmacists are knowledgeable about the drugs they offer. However,
when medical advice is required, consumers would visit a doctor. The contested
services have no relevant commonalities with any of the opponent’s goods. Clearly

Decision on Opposition No B 2 719 998 page: 7 of 12
different by natures and purposes, they do not originate from the same providers and
do not move through the same distribution channels. The mere fact that they can
coincide in the relevant public is not sufficient in itself for a finding of similarity.
Therefore, the contested providing information and advice in the field of animal
healthcare, and veterinary medicine are dissimilar to all of the opponent’s goods.
Remark on the comparison of goods and services
The parties refer to previous decisions of the Office to support their respective
arguments in relation to the comparison of the goods and services. However, the
Office is not bound by its previous decisions as each case has to be dealt with
separately and with regard to its particularities. This practice has been fully supported
by the General Court, which stated that, according to settled case-law, the legality of
decisions is to be assessed purely with reference to the EUTMR, and not to the
Office’s practice in earlier decisions (30/06/2004, T-281/02, Mehr für Ihr Geld,
EU:T:2004:198).
Even though previous decisions of the Office are not binding, their reasoning and
outcome should still be duly considered when deciding upon a particular case. In the
present case, the previous cases referred to by the parties are not relevant to the
present proceedings, as the specifications of the goods and services in question in
the previous cases are factually different. Therefore, the reasoning used in the
previous cases does not apply to the case at hand.
b) Relevant public — degree of attention
The average consumer of the category of products concerned is deemed to be
reasonably well informed and reasonably observant and circumspect. It should also
be borne in mind that the average consumer’s degree of attention is likely to vary
according to the category of goods or services in question.
In the present case, the goods and services found to be identical or similar are
directed at the public at large and at health-care professionals.
The relevant goods and services range from plain, inexpensive medical articles (for
example materials for dressings, disposable syringes) to pharmaceutical
preparations and advisory services related thereto, as well as various specialised
medical articles. Therefore, the relevant public’s degree of attention varies from
average to high, depending on the price, specialised nature, or terms and conditions
of the purchased goods and services.
It is apparent from the case-law that, insofar as pharmaceutical preparations are
concerned, the relevant public’s degree of attention is relatively high, whether or not
issued on prescription (15/12/2010, T-331/09, Tolposan, EU:T:2010:520, § 26;
15/03/2012, T-288/08, Zydus, EU:T:2012:124, § 36 and cited case-law). In particular,
medical professionals have a high degree of attentiveness when prescribing
medicines. Non-professionals also have a higher degree of attention, regardless of
whether the pharmaceuticals are sold without prescription, as these goods affect their
state of health, or that of their pets or livestock.

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c) The signs
Z-MEDICA
Earlier trade mark Contested sign
The relevant territory is the European Union.
The global appreciation of the visual, aural or conceptual similarity of the marks in
question must be based on the overall impression given by the marks, bearing in
mind, in particular, their distinctive and dominant components (11/11/1997, C-251/95,
Sabèl, EU:C:1997:528, § 23).
The unitary character of the European Union trade mark means that an earlier
European Union trade mark can be relied on in opposition proceedings against any
application for registration of a European Union trade mark that would adversely
affect the protection of the first mark, even if only in relation to the perception of
consumers in part of the European Union (18/09/2008, C-514/06 P, Armafoam,
EU:C:2008:511, § 57). This applies by analogy to international registrations
designating the European Union. Therefore, a likelihood of confusion for only part of
the relevant public of the European Union is sufficient to reject the contested
application.
The element ‘Come full circle.’ of the contested sign is meaningful in certain
territories, for example, in those countries where English is understood. The
Opposition Division finds it appropriate to focus the comparison of the signs on the
English-speaking part of the public in the European Union.
The earlier mark comprises two elements, the letter ‘Z’ and the word ‘MEDICA’,
separated by a hyphen. However, none of them is more dominant than the other.
As regards the contested sign, it is co-dominated by the large and centrally
positioned figurative element (‘the clamshell device’ as referred to by the parties) and
the verbal component ‘ZOMEDICA’. In turn, the verbal element ‘Come full circle.’ is
depicted in a marginal position and in a very small size. The meaning that will be
attached to this expression is along the lines of ‘returning to the situation in which you
started, after a series of events or experiences’ (www.collinsdictionary.com). That
reduces the impact of this element in the overall impression of the contested sign,
because consumers will perceive it as a tagline of the main brand, possibly
suggesting that something (for example, the company called ‘ZOMEDICA’) has
returned to its beginnings, has remained faithful to its principles. Consequently, the
public will not attach much trade mark significance to this secondary element.
Although the contested sign’s component ‘ZOMEDICAis a visually undivided block,
the relevant consumers, when perceiving a verbal sign, will break it down into
elements that suggest a concrete meaning, or that resemble words that they already
know (13/02/2007, T-256/04, Respicur, EU:T:2007:46, § 57). Therefore, it can be
reasonably assumed that the relevant public will discern the element ‘MEDICA on
account of the readily perceptible allusion to the concept of ‘medicine’.

Decision on Opposition No B 2 719 998 page: 9 of 12
The applicant argues that the element MEDICAwill be well-known to consumers at
all levels to be a generic reference to the therapeutic properties of the goods and
services. The Opposition Division notes that whilst it cannot be denied that the word
‘MEDICAis derived from the same root as the words ‘medicine’, ‘medical’ etc., and
that in the context of the goods and services a part of the public may even recognise
a reference to the Latin expression ‘materia medica’ which refers to ‘the branch of
medical science concerned with the study of drugs used in the treatment of disease’
(www.collinsdictionary.com), the fact remains that the word ‘MEDICAas such is not
included in common parlance and it does possess a certain degree of fancifulness.
Admittedly, the allusion to the kind of the goods and services renders it weak, but it is
not entirely devoid of distinctiveness in either of the signs in question.
The differentiating parts of the verbal components ‘Z-MEDICA and ‘ZOMEDICAare
the elements ‘Z’ and ‘ZO’, none conveying any clear or evident semantic content for
the relevant public that would go beyond the letters of the English alphabet that they
represent. The parties do not claim that these elements have any meaning either.
Since it can be reasonably assumed that the relevant public will perceive them as
fanciful, these elements enjoy an average degree of distinctiveness.
Although ‘the clamshell device’ of the contested sign is arbitrary and distinctive for
the goods and services at issue, its impact in the overall impression of the contested
sign will be lesser than that of the verbal element ‘ZOMEDICA’. When signs consist
of both verbal and figurative components, in principle, the verbal component of the
sign usually has a stronger impact on the consumer than the figurative component.
This is because the public does not tend to analyse signs and will more easily refer to
the signs in question by their verbal element than by describing their figurative
elements (14/07/2005, T-312/03, Selenium-Ace, EU:T:2005:289, § 37).
Visually, the signs coincide in the letters ‘Z*MEDICA’. This sequence represents the
entirety of the graphemes constituting the earlier mark, and an overwhelming part of
the contested signs element ‘ZOMEDICA’, which does not feature any perceptible
stylisation. The earlier mark differs in that it consists of two elements separated by a
hyphen, and the contested sign differs in the additional letter ‘O’, the figurative
element and the tagline ‘Come full circle.’.
The shared letter sequence is not confined to the component that has limited
distinctiveness, but captures also the initial letter, ‘Z’. The most relevant element of
the contested sign, ‘ZOMEDICA’, differs from the earlier mark in one letter only.
Furthermore, the difference between these verbal elements appears in the same
position, namely in the middle of the shared sequence, ‘Z*MEDICA’.
Bearing in mind the foregoing and also taking into consideration the lesser impact of
the contested sign’s figurative element and the low weight of the element ‘Come full
circle.’, the signs are similar to an average degree.
Aurally, the pronunciations of the signs coincide in the sound of the element
‛MEDICA and their first phonemes, namely the consonant /z/, notwithstanding the
fact that the beginning of the earlier mark may sound like /zed/, /zee/ etc., whereas
the contested sign begins with the sounds corresponding to the letters ‘ZO’.
The applicant argues that the public will immediately perceive that the earlier mark
consists of two parts, whereas the contested sign’s element ‘ZOMEDICAis a single
word, juxtaposed with the relatively long expression ‘Come full circle.’. First, the
Opposition Division notes that ‘Z-MEDICAand ‘ZOMEDICA’ both will be pronounced

Decision on Opposition No B 2 719 998 page: 10 of 12
in four syllables. It is highly unlikely that a perceptible pause would be made on
account of the hyphen in the earlier mark. Second, as regards the presence of the
differentiating element, ‘Come full circle.’, in the contested sign, its weight is limited
for reasons given above. Moreover, due to its subordinate position and size, a
significant part of the public may even skip it when referring to the contested sign.
Since the phonetic coincidences are not confined to the weak element only, as the
tagline has weak distinctiveness, and as the clamshell device of the contested sign
has no impact on the aural level, the signs are similar to an average degree.
Conceptually, although the signs as a whole do not have any clear meaning for the
relevant public, the element ‘MEDICA’, discernible in both signs, will be associated
with the meaning, albeit weak, as explained above. To that extent, the signs are
conceptually similar to a low degree. Neither the arbitrary figurative element, nor the
tagline ‘Come full circle.’ of the contested sign is capable of altering that finding.
As the signs have been found similar in at least one aspect of the comparison, the
examination of likelihood of confusion will proceed.
d) Distinctiveness of the earlier mark
The distinctiveness of the earlier mark is one of the factors to be taken into account
in the global assessment of likelihood of confusion.
The opponent did not explicitly claim that its mark is particularly distinctive by virtue
of intensive use or reputation.
Consequently, the assessment of the distinctiveness of the earlier mark will rest on its
distinctiveness per se. In the present case, the earlier trade mark as a whole has no
clear meaning for any of the goods in question from the perspective of the public in
the relevant language area. Therefore, the distinctiveness of the earlier mark must be
seen as normal, despite the presence of a weak element in the mark as stated above
in section c) of this decision.
e) Global assessment, other arguments and conclusion
Some of the contested goods and services are identical or similar, to varying
degrees, to the opponent’s goods. The similarity between the signs results from the
fact that the entirety of the earlier mark, ‘Z-MEDICA’, shows a perceptible
resemblance to the element ‘ZOMEDICA’ of the contested sign. Admittedly, the signs
feature some differences. Nonetheless, these differences are incapable of removing
the overall impressions produced by the signs sufficiently far as to enable the
average consumer, whether the general public or health-care professionals, to safely
distinguish between them, including where the public displays enhanced attention
when purchasing the goods and services.
Account is taken of the fact that average consumers rarely have the chance to make
a direct comparison between different marks, but must trust in their imperfect
recollection of them (22/06/1999, C-342/97, Lloyd Schuhfabrik, EU:C:1999:323,
§ 26). Even consumers who pay a high degree of attention need to rely on their
imperfect recollection of trade marks (21/11/2013, T-443/12, ancotel, EU:T:2013:605,
§ 54).

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Considering all the above, and based on the average degree of inherent
distinctiveness of the earlier mark, the Opposition Division finds that there is a
likelihood of confusion on the part of the English-speaking part of the public and,
therefore, the opposition is partly well-founded on the basis of the opponent’s
international trade mark registration No 1 045 670 designating the European Union.
As stated above in section c) of this decision, a likelihood of confusion for only part of
the relevant public of the European Union is sufficient to reject the contested
application.
It follows from the above that the contested trade mark must be rejected for the
goods and services found to be identical or similar to those of the earlier trade mark.
As regards the goods and services that have been found to be similar to a low
degree, it is recalled that the evaluating likelihood of confusion implies some
interdependence between the relevant factors and, in particular, a similarity between
the marks and between the goods or services. Therefore, a lesser degree of similarity
between goods and services may be offset by a greater degree of similarity between
the marks and vice versa (29/09/1998, C-39/97, Canon, EU:C:1998:442, § 17). In the
present case, the similarity established between the signs is sufficient to offset the
low degree of similarity found between some of the goods and services, and a
likelihood of confusion exists also in relation to those.
The rest of the contested goods and services, namely all of the services in Class 41
and some of the services in Class 44, are dissimilar. As similarity of goods and
services is a necessary condition for the application of Article 8(1) EUTMR, the
opposition based on this article and directed at these services cannot be successful.
For the sake of completeness, as regards the dissimilar services, the Opposition
Division points out that there is no need to proceed with a comparison of the signs for
the remaining part of the public in the relevant territory, as the outcome of the present
decision would still be the same.
COSTS
According to Article 109(1) EUTMR, the losing party in opposition proceedings must
bear the fees and costs incurred by the other party. According to Article 109(3)
EUTMR, where each party succeeds on some heads and fails on others, or if
reasons of equity so dictate, the Opposition Division will decide a different
apportionment of costs.
Since the opposition is successful only for part of the contested goods and services,
both parties have succeeded on some heads and failed on others. Consequently,
each party has to bear its own costs.

Decision on Opposition No B 2 719 998 page: 12 of 12
The Opposition Division
Birgit FILTENBORG Solveiga BIEZA María Clara
IBÁÑEZ FIORILLO
According to Article 67 EUTMR, any party adversely affected by this decision has a
right to appeal against this decision. According to Article 68 EUTMR, notice of appeal
must be filed in writing at the Office within two months of the date of notification of
this decision. It must be filed in the language of the proceedings in which the decision
subject to appeal was taken. Furthermore, a written statement of the grounds for
appeal must be filed within four months of the same date. The notice of appeal will be
deemed to have been filed only when the appeal fee of EUR 720 has been paid.

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