KLS Martin Manufacturing LLC
ISO 13485:2016 (MDSAP Audit Model Edition 2)
Diese Zertifizierung gehört der Muttergesellschaft 275855 KLS-Martin L. P.
The Design, Planning and Manufacture of patient specific implantable / non-implantable devices and individual patient solution planning (IPS). The design and manufacture of non-active re-usable surgical instruments. - USA (a,b,c,d) REPs FEI No.: F005984