Laboratorios Bago de Bolivia
Os Laboratórios Bago de Bolívia fabricam produtos farmacêuticos para canais regionais B2B.
Os Laboratórios Bago de Bolivia fabricam produtos farmacêuticos, medicamentos prescritos e formulações para cuidados de saúde em La Paz. Fundada em 1976, a empresa fornece farmácias, hospitais, atacadistas médicos e parceiros de exportação em BO, PE, CL, AR e mercados de exportação relacionados.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- La Paz, Bolivia
- Founded
- 1976
- Website
- bago.com.bo
- Categories
- Suprimentos médicos e de saúde
- Markets
- Bolívia, Peru, Chile, Argentina
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
- corporate-mail-on-domain (green), checked 2026-08-05 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-05 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- web-presence-since (green), checked 2026-08-05 Internet Archive (Wayback)
- product-authorised-for-sale (green), checked 2026-08-22 Agencia Estatal de Medicamentos y Tecnologias en Salud (AGEMED, Bolivia), listado oficial de registros sanitarios aprobados
- debarment-clear (green), checked 2026-08-05 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- registered-manufacturer (green), checked 2026-08-22 Agencia Estatal de Medicamentos y Tecnologias en Salud (AGEMED, Bolivia), listado oficial de registros sanitarios aprobados
Import rules for these goods
- 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)