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House mark for medical devices (term considered too vague by the International Bureau pursuant to Rule 13 (2) (b) of the Regulations) and medical apparatus in the field of diabetes; medical apparatus and instruments for diabetes management use; medical devices and apparatus for diagnosis, monitoring, and treatment of diabetes; medical ports, lancets, needles and syringes; kits for diabetic patients comprised of syringes or pen needles; clipper used for destruction of medical needles; scale magnifier and needle guide for insulin syringes; pen needles used to deliver medications to manage diabetes; infusion sets; infusion set accessories, namely, belt clips specifically designed for holding infusion pumps and infusion sets; subcutaneous infusion sets for use by diabetes patients in connection with insulin pumps; infusion pumps; insulin pumps; infusion and insulin pump accessories, medical sensors, meters and devices for measuring and monitoring blood and urine properties, and accessories therefor; glucose meters; blood glucose meters; medical apparatus for monitoring blood glucose levels; medical apparatus and instruments for monitoring glucose; continuous glucose monitoring systems composed of medical apparatus for monitoring glucose; sensor-based glucose monitors for medical purposes; blood glucose monitoring systems including the devices, and parts and accessories thereof, namely, blood glucose monitoring carrying cases, and electronic blood glucose test diaries in the nature of integrated memory components within blood glucose monitors; blood glucose monitoring system accessories; devices for monitoring blood glucose for medical purposes; devices for measuring blood sugar; medical devices, namely, medical sensors that are implanted or inserted into the human body used to continuously monitor the concentration of glucose in the human body and accessories therefor, namely, receivers, sensor housings and sensor insertion devices; medical diagnostic apparatus for testing blood sugar levels incorporating recorded software for the collection, editing, organizing, modifying, transmission, storage and sharing of medical information (term considered too vague by the International Bureau pursuant to Rule 13 (2) (b) of the Regulations).