Benta Pharma Industries
1994'ten bu yana 40'tan fazla ülkede faaliyet gösteren farmasötik ve steril tıbbi cihaz üreticisi.
Benta Pharma Industries, CNS, kardiyovasküler ve metabolik durumlara yönelik geliştirilmiş farmasötik formülasyonların yanı sıra göz içi lensler ve IV uygulama setleri dahil olmak üzere steril tıbbi cihazlar da üretmektedir. 1994 yılında kurulan ve merkezi Lübnan'da bulunan, Lübnan ve Mısır'daki fabrikaları bulunan Benta Grubu, Suudi Arabistan, Irak, Mısır ve Fransa'daki bölge ofisleri ile 40'tan fazla ülkede faaliyet göstermektedir.
- 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
- Tıbbi ve Sağlık Malzemeleri
- Markets
- Suudi Arabistan, Irak, Mısır, Fransa, Birleşik Arap Emirlikleri
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)