1.

Does the advertising, as set out in Annex K2 to the application of 1 September 2023 (page 16 et seq. of the electronic file), for the patient wristbands at issue – in respect of which it is not disputed that they were supplied without anything printed thereon – produced by the US manufacturer Zebra Technologies Corp. contain an intended purpose within the meaning of Article 2(12) of Regulation (EU) 2017/745? (1)

2.

In the event that the answer to question 1 is in the affirmative:

Are the patient wristbands at issue – in respect of which it is not disputed that they were supplied without anything printed thereon – produced by the US manufacturer Zebra Technologies Corp. of the types ‘Direct Thermal Wristband Z-Band Ultrasoft’ (Part. No. 10018856) and ‘LaserBand Advanced’– as depicted in Annex K1 to the application of 1 September 2023 (page 9 et seq. of the electronic file) – offered by the defendant as ‘Patientenarmband ThermoComfort PLUS (Patient wristband ThermoComfort PLUS) (Article 511621)’ and ‘Patientenarmband LaserBand A4 ungestanzt “Erwachsene” mit Schutzfolie’ (Patient wristband LaserBand A4 unpunched ‘Adult’ with protective foil) (Article 512099)’ and advertised by the manufacturer Zebra Technologies Corp. as set out in Annex K2 to the application of 1 September 2023 (page 16 et seq. of the electronic file), medical devices within the meaning of Article 2(1) of Regulation 2017/745?