Qualified source record ยท not independently verified
CARIBBEAN MANUFACTURING SAS is listed in FDA device registration data in Cartagena Bolivar, CO with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Qualified source record ยท not independently verified
INNOVATIVE MEDICAL TECH SAS is listed in FDA device registration data in Baranquilla Atlantico, CO with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Qualified source record ยท not independently verified
KAMEX INTERNATIONAL S.A.S is listed in FDA device registration data in Cajica Cundinamarca, CO with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Qualified source record ยท not independently verified
MACROLAB ASOCIADOS S.A.S. is listed in FDA device registration data in MEDELLIN Antioquia, CO with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Qualified source record ยท not independently verified
MEDI VARIC PRODUCTS SAS is listed in FDA device registration data in Bogota, CO with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Qualified source record ยท not independently verified
PILAB S.A.S. is listed in FDA device registration data in Bogota, CO with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Qualified source record ยท not independently verified
RONEXMED S.A.S. is listed in FDA device registration data in Barranquilla Atlantico, CO with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Qualified source record ยท not independently verified
VYGON COLOMBIA S.A. is listed in FDA device registration data in BARRANQUILLA Atlantico, CO with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Profiles identify their evidence level. A qualified source record is not an independently verified supplier, certification, capacity statement or recommendation. How we research suppliers