Benta Pharma Industries
Producent farmaceutyków i sterylnych wyrobów medycznych obecny w ponad 40 krajach od 1994 roku.
Benta Pharma Industries produkuje ulepszone preparaty farmaceutyczne stosowane w leczeniu chorób OUN, układu sercowo-naczyniowego i metabolicznego, a także sterylne wyroby medyczne, w tym soczewki wewnątrzgałkowe i zestawy do podawania dożylnego. Założona w 1994 roku z siedzibą w Libanie i zakładami w Libanie i Egipcie, Grupa Benta działa w ponad 40 krajach z biurami regionalnymi w Arabii Saudyjskiej, Iraku, Egipcie i Francji.
- 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
- Artykuły medyczne i związane z opieką zdrowotną
- Markets
- Arabia Saudyjska, Irak, Egipt, Francja, Zjednoczone Emiraty Arabskie
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)