Benta Pharma Industries
Fabrikant van farmaceutische en steriele medische hulpmiddelen, sinds 1994 aanwezig in meer dan 40 landen.
Benta Pharma Industries produceert verbeterde farmaceutische formuleringen voor CZS-, cardiovasculaire en metabolische aandoeningen, evenals steriele medische hulpmiddelen, waaronder intraoculaire lenzen en IV-toedieningssets. De Benta Group, opgericht in 1994 en met hoofdkantoor in Libanon en fabrieken in Libanon en Egypte, is actief in meer dan 40 landen met regionale kantoren in Saoedi-Arabië, Irak, Egypte en Frankrijk.
- 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
- Medische en gezondheidszorgbenodigdheden
- Markets
- Saoedi-Arabië, Irak, Egypte, Frankrijk, Verenigde Arabische Emiraten
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)