Medical Device Contract Manufacturers
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Qualified source record · not independently verified
SHIGA SHOFU INC. is listed in FDA device registration data in Koka Shiga, JP 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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SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION is listed in FDA device registration data in KYOTO Ky?to, JP 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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SHIMA LABORATORIES CO., LTD. is listed in FDA device registration data in ITABASHI-KU T?ky?, JP 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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SHIMANE SHIMADZU CORPORATION is listed in FDA device registration data in IZUMO Shimane, JP 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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SHINCOTEC CO., LTD. is listed in FDA device registration data in Kawagoe Saitama, JP 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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Sony Global Manufacturing & Operations Corporation Kohda Site is listed in FDA device registration data in Nukata-gun Aichi, JP 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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SORD CORPORATION is listed in FDA device registration data in Chiba-Shi T?ky?, JP 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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SUNREEVE CO., LTD. is listed in FDA device registration data in SABAE, FUKUI, JP 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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SUZUYO CO., LTD is listed in FDA device registration data in Yokohama Kanagawa, JP 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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TAISEI KAKO CO., LTD. is listed in FDA device registration data in Ibaraki ?saka, JP 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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TAIYO KOGYO CO., LTD. HANYU TECHNICAL PLANT is listed in FDA device registration data in Hanyu Saitama, JP 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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Takahata Electronics Corporation is listed in FDA device registration data in YONEZAWA Yamagata, JP 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
Japan