Benta Pharma Industries
自 1994 年以来，制药和无菌医疗器械制造商在 40 多个国家/地区开展业务。
Benta Pharma Industries 生产用于中枢神经系统、心血管和代谢疾病的增强型药物制剂以及无菌医疗设备，包括人工晶状体和静脉注射装置。 Benta 集团成立于 1994 年，总部位于黎巴嫩，在黎巴嫩和埃及设有工厂，业务遍及 40 多个国家，并在沙特阿拉伯、伊拉克、埃及和法国设有区域办事处。
- 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
- 医疗保健用品
- Markets
- 沙特阿拉伯, 伊拉克, 埃及, 法国, 阿拉伯联合酋长国
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)