Laboratorios Bagó S.A.
Argentine pharmaceutical and nutraceutical manufacturer exporting to 40+ countries since 1934.
Laboratorios Bagó is one of Argentina's largest independent pharmaceutical manufacturers, founded in 1934 in Buenos Aires and producing prescription drugs, OTC medicines, dermatological products, and nutritional supplements. The company exports to more than 40 countries across Latin America, the United States, and Eastern Europe through affiliate companies and wholesale distributors, operating GMP-certified plants in Buenos Aires and subsidiary facilities in Brazil, Chile, and Mexico. Its broad product range, long regulatory track record, and established regional distribution make Bagó a key B2B supplier for pharmaceutical importers and hospital group procurement in the Americas.
- 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
- Medical & Healthcare Supplies, Supplements & Wellness
- Markets
- Argentina, Brazil, Chile, Mexico, Peru, Colombia, United States
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)