Laboratorios Bago de Bolivia
Laboratorios Bago de Bolivia는 지역 B2B 채널을 위한 의약품을 제조합니다.
Laboratorios Bago de Bolivia는 라파스에서 의약품, 처방약 및 건강 관리 제제를 제조합니다. 1976년에 설립된 이 회사는 BO, PE, CL, AR 및 관련 수출 시장 전반에 걸쳐 약국, 병원, 의료 도매업체 및 수출 파트너에게 제품을 공급합니다.
- 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
- 의료 및 건강 관리 용품
- Markets
- 볼리비아, 페루, 칠레, 아르헨티나
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)