Benta Pharma Industries
Fabricante de dispositivos médicos farmacêuticos e estéreis presente em mais de 40 países desde 1994.
A Benta Pharma Industries fabrica formulações farmacêuticas aprimoradas para condições do SNC, cardiovasculares e metabólicas, bem como dispositivos médicos estéreis, incluindo lentes intraoculares e conjuntos de administração intravenosa. Fundado em 1994 e sediado no Líbano com fábricas no Líbano e no Egito, o Grupo Benta atua em mais de 40 países com escritórios regionais na Arábia Saudita, Iraque, Egito e França.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Beirut, Lebanon
- Founded
- 1994
- Website
- bpi.com.lb
- Categories
- Suprimentos médicos e de saúde
- Markets
- Arábia Saudita, Iraque, Egito, França, Emirados Árabes 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
- domain-registered (green), checked 2026-08-06 Domain registry record
- 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
- certificate-page-on-site (amber), checked 2026-09-18 Company's own certification page
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
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)