Medical Device Contract Manufacturers
Compare qualified profiles associated with japan. Check each record's evidence level before discussing your project.
Qualified source record · not independently verified
A&D Manufacturing Company, Limited - Tsukuba Factory is listed in FDA device registration data in Shimotsuma-shi Ibaraki, 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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AIR WATER REALIZE INC. is listed in FDA device registration data in IWAKI-SHI Fukushima, 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 →Qualified source record · not independently verified
AIR WATER REALIZE INC. is listed in FDA device registration data in Kasama-shi Ibaraki, 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 →Qualified source record · not independently verified
AITEC CO., LTD. is listed in FDA device registration data in OZU-SHI Ehime, 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 →Qualified source record · not independently verified
Akita Sumitomo Bakelite Co., Ltd. is listed in FDA device registration data in Akita, 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 →Qualified source record · not independently verified
AOMI PRECISION CO. LTD. is listed in FDA device registration data in NIIGATA, 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 →Qualified source record · not independently verified
Aomori Olympus Co., Ltd. Hirosaki Site is listed in FDA device registration data in Hirosaki-shi Aomori, 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 →Qualified source record · not independently verified
AOMORI OLYMPUS CO., LTD. Kuroishi Site is listed in FDA device registration data in KUROISHI-SHI Aomori, 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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Asahi Kasei Medical MT Corp. Oita Works is listed in FDA device registration data in OITA-SHI ?ita, 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 →Qualified source record · not independently verified
ASAHI POLYSLIDER COMPANY, LIMITED Okayama-Kuse Plant is listed in FDA device registration data in Maniwa Okayama, 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 →Qualified source record · not independently verified
ASHITAKA FACTORY OF TERUMO CORP. is listed in FDA device registration data in FUJINOMIYA Shizuoka, 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 →Qualified source record · not independently verified
ATEX CO., LTD. is listed in FDA device registration data in Osaka ?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.
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