Benta Pharma Industries
1994 年以来 40 か国以上で展開している医薬品および滅菌医療機器のメーカー。
Benta Pharma Industries は、CNS、心血管、代謝疾患向けの強化された医薬製剤のほか、眼内レンズや点滴投与セットなどの滅菌医療機器を製造しています。 1994 年に設立され、レバノンに本社を置き、レバノンとエジプトに工場を置くベンタ グループは、サウジアラビア、イラク、エジプト、フランスに支社を置き、40 か国以上で活動しています。
- 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
- 医療およびヘルスケア用品
- Markets
- サウジアラビア, イラク, エジプト, フランス, アラブ首長国連邦
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)