Medical Device Contract Manufacturers
Compare qualified profiles associated with finland. Check each record's evidence level before discussing your project.
Qualified source record · not independently verified
AirLife Finland Oy is listed in FDA device registration data in Helsinki Uusimaa, FI 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.
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ARCTIC BIOMATERIALS OY is listed in FDA device registration data in Tampere Pirkanmaa, FI 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.
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INION OY is listed in FDA device registration data in TAMPERE Pirkanmaa, FI 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.
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INNOKAS MEDICAL OY is listed in FDA device registration data in KEMPELE Pohjois-Pohjanmaa, FI 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.
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KB Components Finland Oy is listed in FDA device registration data in Nurmijarvi Etela-Karjala, FI 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.
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KYTOLA INSTRUMENTS OY is listed in FDA device registration data in Muurame Keski-Suomi, FI 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.
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LM-INSTRUMENTS OY is listed in FDA device registration data in PARAINEN Varsinais-Suomi, FI 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.
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MARIACHI OY is listed in FDA device registration data in Littoinen Varsinais-Suomi, FI 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.
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MECTALENT LTD. is listed in FDA device registration data in Oulu Kainuu, FI 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.
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MODULIGHT CORPORATION is listed in FDA device registration data in Tampere Pirkanmaa, FI 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.
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OY PRIMO FINLAND AB is listed in FDA device registration data in Vaasa Pohjanmaa, FI 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.
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SCREENTEC OY is listed in FDA device registration data in Oulu, Finland Pohjois-Pohjanmaa, FI 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.
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Finland