© uma Schreibgeräte Ullmann GmbH
The uma GREEN range is ideal for marketing and communication activities in the healthcare and medical sectors.
Promote with ICON GREEN, EFFECT GREEN und PIXEL F GREEN not only antibacterial, but consciously rely on further positive arguments for an environmentally conscious, safe and sustainable uma writing instrument production.
The writing instruments are made of an antibacterial plastic. An antimicrobial additive in the form of silver ions is added to the ABS plastic. An adhesion and settlement of bacteria or pathogens on the surface of the writing instruments is prevented or reduced.
The writing instruments are produced in Europe and finished climate neutral in the Black Forest. In this way, an additional positive contribution to the environment is made.
It does not contain dioxin, phthalates, biosphenol A, antimony, arsenic, barium, cadmium, chrome, mercury, lead, polybrominated biphenyls (PBBs), polybrominated diphenyl ethers (PBDEs) or deca-BDE, and conforms to RoHS and REACH directives.
The used plastic meets European and American FDA regulations for contact with foodstuffs.
Non-hazardous according to the regulation on classification, labelling and packaging of substances and mixtures.
Laboratory tests have shown that up to 99.99% of bacteria and pathogens on the surface of writing instruments are destroyed. Tested according to ISO 22196:2011, the antibacterial effect is guaranteed for the entire life of the writing instrument and thus offers lasting protection.
Made of non-toxic plastic, the writing instrument was developed for a particularly long durability. The risk, that harmful substances are released into the environment is thereby minimized. Using this pen as long as possible helps us to reduce environmental pollution and thus underlines the idea of sustainable advertising.
Short and fast delivery routes enable reliable and short-term production and create an additional contribution to the preservation to the environment.
Made of plastic suitable for toys (according to European standard EN 71, part 3 and US FDA regulations).