Medilar Importação e Distribuição

独立来源是否相符？

关于

Medilar 进口和分销药品和保健品。其维拉克鲁斯总部支持区域配送中心，为巴西各地的机构客户提供服务。

品类

药品制造医疗保健用品

主要市场

🇧🇷 巴西

探索

巴西 的分销商巴西 的 药品制造巴西 的 医疗保健用品

适用于这些商品的规则

本行业货运通常适用的法规。并非法律意见：请以链接的官方来源为准。

• 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)
• Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)

分销能力

合作角色

Importer / ExporterMaster / Exclusive DistributorDistributor

覆盖国家

🇧🇷 巴西

销售渠道

Wholesale & Cash-and-CarryInstitutional & Government Procurement

客户类型

Healthcare Facilities (Hospitals & Clinics)Pharmacies & Health StoresInstitutional & Corporate Buyers