Benta Pharma Industries
1994년부터 40개국 이상에 진출한 제약 및 멸균 의료 기기 제조업체입니다.
Benta Pharma Industries는 CNS, 심혈관 및 대사 질환을 위한 향상된 약품 제제는 물론 안구내 렌즈 및 IV 투여 세트를 포함한 멸균 의료 기기를 제조합니다. 1994년에 설립되어 레바논에 본사를 두고 레바논과 이집트에 공장을 두고 있는 Benta Group은 사우디아라비아, 이라크, 이집트, 프랑스에 지역 사무소를 두고 40개국 이상에서 활동하고 있습니다.
- 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
- 의료 및 건강 관리 용품
- Markets
- 사우디아라비아, 이라크, 이집트, 프랑스, 아랍에미리트
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)