Qualified source record ยท not independently verified
Bien-Air Portugal Unipessoal LDA is listed in FDA device registration data in Maia Porto, PT 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.
Qualified source record ยท not independently verified
ENERGYPULSE SYSTEMS is listed in FDA device registration data in Lisboa, PT 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.
Qualified source record ยท not independently verified
K Line Portugal Unipessoal Ltd is listed in FDA device registration data in Chaves Braga, PT 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.
Qualified source record ยท not independently verified
LX PRECISION PORTUGAL, UNIPESSOAL, LDA is listed in FDA device registration data in Castelo de Paiva Aveiro, PT 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.
Qualified source record ยท not independently verified
Shamir Portugal is listed in FDA device registration data in VCD Porto, PT 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.
Profiles identify their evidence level. A qualified source record is not an independently verified supplier, certification, capacity statement or recommendation. How we research suppliers