Laboratorios Bagó S.A.
Fabricante argentino de productos farmacéuticos y nutracéuticos que exporta a más de 40 países desde 1934.
Laboratorios Bagó es uno de los fabricantes farmacéuticos independientes más grandes de Argentina, fundado en 1934 en Buenos Aires y que produce medicamentos recetados, medicamentos de venta libre, productos dermatológicos y suplementos nutricionales. La empresa exporta a más de 40 países de América Latina, Estados Unidos y Europa del Este a través de empresas filiales y distribuidores mayoristas, operando plantas certificadas GMP en Buenos Aires e instalaciones subsidiarias en Brasil, Chile y México. Su amplia gama de productos, su larga trayectoria regulatoria y su distribución regional establecida hacen de Bagó un proveedor B2B clave para importadores farmacéuticos y adquisiciones de grupos hospitalarios en las Américas.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Buenos Aires, Argentina
- Founded
- 1934
- Website
- bago.com.ar
- Categories
- Suministros médicos y sanitarios, Suplementos y bienestar
- Markets
- Argentina, Brasil, Chile, México, Perú, Colombia, Estados Unidos
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- product-authorised-for-sale (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
- domain-registered (green), checked 2026-08-11 Domain registry record
- registered-manufacturer (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
- market-access-eu (green), checked 2026-08-22 TRACES NT, European Commission register of approved establishments (DG SANTE)
- debarment-clear (green), checked 2026-08-06 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-06 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-06 Mail server of the company domain
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- Food supplements sold in the EU follow Directive 2002/46/EC: most member states require a notification to the national authority before the first sale. European Commission (supplements)
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)