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Document 62016CA0642

Case C-642/16: Judgment of the Court (Fifth Chamber) of 17 May 2018 (request for a preliminary ruling from the Bundesgerichtshof, Germany) — Junek Europ-Vertrieb GmbH v Lohmann & Rauscher International GmbH & Co. KG (Reference for a preliminary ruling — Intellectual property — Trade-mark law — Regulation (EC) No 207/2009 — Article 13 — Exhaustion of the rights conferred by a trade mark — Parallel imports — Repackaging of the product bearing the mark — New labelling — Conditions applicable to medical devices)

OJ C 240, 9.7.2018, p. 5–5 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

201806220251970762018/C 240/066422016CJC24020180709EN01ENINFO_JUDICIAL201805175511

Case C-642/16: Judgment of the Court (Fifth Chamber) of 17 May 2018 (request for a preliminary ruling from the Bundesgerichtshof, Germany) — Junek Europ-Vertrieb GmbH v Lohmann & Rauscher International GmbH & Co. KG (Reference for a preliminary ruling — Intellectual property — Trade-mark law — Regulation (EC) No 207/2009 — Article 13 — Exhaustion of the rights conferred by a trade mark — Parallel imports — Repackaging of the product bearing the mark — New labelling — Conditions applicable to medical devices)

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C2402018EN510120180517EN00065151

Judgment of the Court (Fifth Chamber) of 17 May 2018 (request for a preliminary ruling from the Bundesgerichtshof, Germany) — Junek Europ-Vertrieb GmbH v Lohmann & Rauscher International GmbH & Co. KG

(Case C-642/16) ( 1 )

‛(Reference for a preliminary ruling — Intellectual property — Trade-mark law — Regulation (EC) No 207/2009 — Article 13 — Exhaustion of the rights conferred by a trade mark — Parallel imports — Repackaging of the product bearing the mark — New labelling — Conditions applicable to medical devices)’

2018/C 240/06Language of the case: German

Referring court

Bundesgerichtshof

Parties to the main proceedings

Applicant: Junek Europ-Vertrieb GmbH

Defendant: Lohmann & Rauscher International GmbH & Co. KG

Operative part of the judgment

Article 13(2) of Council Regulation (EC) No 207/2009 of 26 February 2009 on the European Union trade mark must be interpreted as meaning that the proprietor of a mark cannot oppose the further commercialisation, by a parallel importer, of a medical device in its original internal and external packaging where an additional label, such as that at issue in the case in the main proceedings, has been added by the importer, which, by its content, function, size, presentation and placement, does not give rise to a risk to the guarantee of origin of the medical device bearing the mark.


( 1 ) OJ C 104, 3.4.2017.

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