Benta Pharma Industries
Produsen peralatan medis farmasi dan steril hadir di 40+ negara sejak tahun 1994.
Benta Pharma Industries memproduksi formulasi farmasi yang disempurnakan untuk kondisi SSP, kardiovaskular, dan metabolisme serta perangkat medis steril termasuk lensa intraokular dan perangkat pemberian IV. Didirikan pada tahun 1994 dan berkantor pusat di Lebanon dengan pabrik di Lebanon dan Mesir, Benta Group aktif di lebih dari 40 negara dengan kantor regional di Arab Saudi, Irak, Mesir, dan Prancis.
- 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
- Perlengkapan Medis & Kesehatan
- Markets
- Arab Saudi, Irak, Mesir, Prancis, Uni Emirat Arab
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)