Medical Device Contract Manufacturers
Supplier directory
Find a manufacturing partner by capability, industry and company location.
Liege Liege,
BelgiumQualified source record ยท not independently verified
Immunodiagnostic Systems SA is listed in FDA device registration data in Liege Liege, BE 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.
Request supplier options โVerviers Liege,
BelgiumQualified source record ยท not independently verified
Lonza Verviers SRL. is listed in FDA device registration data in Verviers Liege, BE 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.
Request supplier options โAngleur Liege,
BelgiumQualified source record ยท not independently verified
MEDI-LINE S.A. is listed in FDA device registration data in Angleur Liege, BE 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.
Request supplier options โPuurs-Sint-Amands Antwerpen,
BelgiumQualified source record ยท not independently verified
Novartis Manufacturing NV is listed in FDA device registration data in Puurs-Sint-Amands Antwerpen, BE 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.
Request supplier options โBuggenhout Oost-Vlaanderen,
BelgiumQualified source record ยท not independently verified
Ontex BV is listed in FDA device registration data in Buggenhout Oost-Vlaanderen, BE 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.
Request supplier options โEeklo Oost-Vlaanderen,
BelgiumQualified source record ยท not independently verified
Ontex Eeklo is listed in FDA device registration data in Eeklo Oost-Vlaanderen, BE 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.
Request supplier options โLichtervelde West-Vlaanderen,
BelgiumQualified source record ยท not independently verified
OPTIMAT (AFDELING HUIZE TORDALE VZW) is listed in FDA device registration data in Lichtervelde West-Vlaanderen, BE 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.
Request supplier options โWIJNEGEM Antwerpen,
BelgiumQualified source record ยท not independently verified
ORFIT INDUSTRIES NV is listed in FDA device registration data in WIJNEGEM Antwerpen, BE 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.
Request supplier options โGEMBLOUX Namur,
BelgiumQualified source record ยท not independently verified
SURGICAL INSTRUMENTS BELGIUM SA is listed in FDA device registration data in GEMBLOUX Namur, BE 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.
Request supplier options โLeuven Vlaams Brabant,
BelgiumQualified source record ยท not independently verified
Terumo BCT Europe N.V. is listed in FDA device registration data in Leuven Vlaams Brabant, BE 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.
Request supplier options โMeulebeke West-Vlaanderen,
BelgiumQualified source record ยท not independently verified
TWE Meulebeke NV is listed in FDA device registration data in Meulebeke West-Vlaanderen, BE 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.
Request supplier options โProfiles identify their evidence level. A qualified source record is not an independently verified supplier, certification, capacity statement or recommendation. How we research suppliers