The products developed, Distributed by Globmed belong to the category of Single Use Medical Devices & Implantable Medical Devices pursuant to European Directive 93/42/EEC amended by directive 2007/47/EEC.

The company’s industrial credibility routinely involves monitoring a comprehensive and thorough quality system compliant with EN ISO 13485 (specific for medical devices). Globmed Holding was awarded EN ISO 9001, 13485 certification.

All Globmed Holding Distributed products have been awarded the CE mark by Notified Bodies, guaranteeing compliance with European production, traceability, safety, labeling and packaging specifications.

Due to the high quality requirements and advanced technology, Globmed Holding is attentive to its users’ needs and to patient comfort.