Med Center Comercial

独立来源是否相符？

关于

Med Center Commercial 经销药品和保健品。它为巴西的药房和医疗机构提供服务。

品类

医疗保健用品药品制造

主要市场

🇧🇷 巴西

探索

巴西 的分销商巴西 的 医疗保健用品巴西 的 药品制造

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

DistributorWholesaler

覆盖国家

🇧🇷 巴西

销售渠道

Wholesale & Cash-and-CarryInstitutional & Government Procurement

客户类型

Pharmacies & Health StoresHealthcare Facilities (Hospitals & Clinics)