SALF is authorized to produce, package, test and sale medical devices of Class I, IIa, IIb and III.
The Istituto Superiore di Sanità (National Institute of Health), Notified Body no. 0373, certifies that the assurance system of quality, manufacturing and sterilization of S.A.L.F. for medical devices complies with the requirements of the European Directive 93/42/EEC.