Medical Device Contract Manufacturers
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Qualified source record · not independently verified
Arrow International C.R. a.s. is listed in FDA device registration data in ZDAR NAD SAZAVOU Vyso?ina, CZ 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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Arrow International CR, a.s. is listed in FDA device registration data in Hradec Kralove Hradec Kralove, CZ 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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AVEFLOR is listed in FDA device registration data in Kopidlno Ji?in, CZ 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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CIMPAX CZ s.r.o. is listed in FDA device registration data in Vyskov Vyskov, CZ 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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CONNECTRONICS S.R.O. is listed in FDA device registration data in Kladno Kladno, CZ 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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CONTRACT MEDICAL INTERNATIONAL, SPOL. S R.O. is listed in FDA device registration data in Hradec Kralove Hradec Kralove, CZ 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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DEYMED DIAGNOSTIC S.R.O. is listed in FDA device registration data in Hronov Nachod, CZ 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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DINA-HITEX, spol. s r.o. is listed in FDA device registration data in Bucovice Vyskov, CZ 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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DRYLOCK TECHNOLOGIES S.R.O. is listed in FDA device registration data in Hradek nad Nisou Liberecky Kraj, CZ 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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EH Labs CZ s.r.o. is listed in FDA device registration data in Dvur Kralove nad Labem Hradec Kralove, CZ 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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ELLA-CS, S.R.O. is listed in FDA device registration data in Hradec Kralove Hradec Kralove, CZ 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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EXBIO PRAHA, A.S. is listed in FDA device registration data in Vestec Praha-Zapad, CZ 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
Czechia