1984
Clinical trials on Solutran compound formulations and launch in the market of bags filled with infusion solutions, Pierrel Hospital becomes a leader on the domestic market
1986
Important clinical trials of Solutran is carried out on containers filled with infusion solutions with bicarbonate
1988
Born of MGS Medical Grade System, the industrial company that focuses on the development of all possible applications of the compound of the Medical grade Solutran for the filling of empty bags in infusion solutions, the production of tubular semi-finished products and medical grade tubes, Empty bags for infusional use
2000
The company completes all Quality Certifications in accordance with UNI EN ISO 9001: 2000, develops and obtains CE Certification for various medical devices medical devices: blood deflators and transfusers, and in particular for a special container used for control Of blood loss during the delivery phase, obtaining the CE mark of the device, with the trademark Kifarm
2005
MGS – Medical Grade System – is acquired by Meditalia Srl, which pursues to develope the established tradition and know-how in international hospitals and pharmaceutical companies
2014
Successfully complete clinical trials on the hemo, compound, tubular and bags of Solutran for the production of bags for the containment and fractionation of human blood, obtaining excellent results in relation to the state of the art, accredited by the Policlinico di Milano transfusion center which led the study. R&D and manufactures a new PVC-free monolayer compound, branded Solucare for PVC-free PVC bags and tubes.
2009
The company renews its Quality Certifications by adapting the regulations in accordance with UNI EN 1SO 9001: 2008.
It launches the clinical trial on the compound, raw material and bags for the containment and fractionation of blood for human use by developing the medical grade compound – Solutran hemo. R&D and realize the tubular NutriEva used for the production of bags for the Nutrition sector. R&D a particular compound, Solutran G, used for drainage bags and for the Blood Management sector. R&D a particular Kit, Solutran hemo O2O3 for the administration of a blend of ozone in autologous hematology.
2016
The company renews Certifications by adapting the regulations in accordance with ISO 9001: 2008; UNI EN ISO 13485: 2003.
R&D a patent in co-operation with the Fondazione Cà Granda – Hospital Maggiore Policlinico, for a special kit in the preparation and administration of a platelet concentrate obtained from the cordonal blood
2017
After obtaining the CE certificate at the end of 2016, the company officially launches the SOLUTRAN® Hemo Blood Bags.
2018
The company renews the certification of the quality management system UNI EN ISO 13485: 2016. Furthermore it obtains the CE certificate which will be the starting for the launch on the world market of the SOLUTRAN® Hemo Accessory Bags and of the new BioNest System patented by Meditalia with the collaboration of the CaGranda Foundation – Ospedale Maggiore Policlinico of Milan.
2019
To complete the BioNest System line, a new product has been developed specifically for the preparation of multiple aliquots of platelet gel from adult donor platelets. Meditalia patent already covered by CE certification.