Medical Device Contract Manufacturers
Compare qualified profiles associated with greece. Check each record's evidence level before discussing your project.
Qualified source record · not independently verified
CAMARK SA is listed in FDA device registration data in Axioupoli Kentriki Makedonia, GR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
DMP Dental Industry S.A. is listed in FDA device registration data in Markopoulo Attiki, GR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
GALENICA PHARMACEUTICAL I.S.A. is listed in FDA device registration data in Kifissia Attiki, GR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
GREEK HANDMADE FRAMES SA is listed in FDA device registration data in KRIONERI Attiki, GR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
MEDICON HELLAS SA is listed in FDA device registration data in GERAKAS Attiki, GR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
VITROMED SMPC is listed in FDA device registration data in Ilion Attiki, GR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Profiles identify their evidence level. A qualified source record is not an independently verified supplier, certification, capacity statement or recommendation. How we research suppliers
Greece