Heverlee Vlaams Brabant,
BelgiumQualified source record ยท not independently verified
3D SYSTEMS - LAYERWISE is listed in FDA device registration data in Heverlee 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 โMortsel Antwerpen,
BelgiumQualified source record ยท not independently verified
Agfa Gevaert N.V. is listed in FDA device registration data in Mortsel 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 โAarschot Flanders,
BelgiumQualified source record ยท not independently verified
AMNOVIS BV is listed in FDA device registration data in Aarschot Flanders, 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 โLommel Limburg,
BelgiumQualified source record ยท not independently verified
Aqua free Industries BV is listed in FDA device registration data in Lommel Limburg, 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 โMarche-en-Famenne Luxembourg,
BelgiumQualified source record ยท not independently verified
Beldico S.A. is listed in FDA device registration data in Marche-en-Famenne Luxembourg, 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 โMechelen Antwerpen,
BelgiumQualified source record ยท not independently verified
BIOCARTIS NV is listed in FDA device registration data in Mechelen 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 โWellen Limburg,
BelgiumQualified source record ยท not independently verified
BIONCISE NV is listed in FDA device registration data in Wellen Limburg, 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 โHeist-op-den-Berg Antwerpen,
BelgiumQualified source record ยท not independently verified
COSMADE BELGIUM BV is listed in FDA device registration data in Heist-op-den-Berg 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 โHamont-Achel Limburg,
BelgiumQualified source record ยท not independently verified
ENESTIA BELGIUM NV (SHARP BELGIUM) is listed in FDA device registration data in Hamont-Achel Limburg, 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 โMOL Antwerpen,
BelgiumQualified source record ยท not independently verified
EYE SPECIALS INTERNATIONAL is listed in FDA device registration data in MOL 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 โBEERNEM West-Vlaanderen,
BelgiumQualified source record ยท not independently verified
FERTIPRO N.V. is listed in FDA device registration data in BEERNEM 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 โGHENT Oost-Vlaanderen,
BelgiumQualified source record ยท not independently verified
Fujirebio Europe N.V. is listed in FDA device registration data in GHENT 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 โProfiles identify their evidence level. A qualified source record is not an independently verified supplier, certification, capacity statement or recommendation. How we research suppliers