Urufarma S.A.
乌拉圭制药商，自 1946 年起专门生产激素和肿瘤产品
Urufarma 是一家总部位于蒙得维的亚的制药商，生产激素产品、口服避孕药和肿瘤药物，出口到 50 多个国家。该公司拥有 GLP 认证，最近在卡拉斯科机场附近开设了一个新的工业综合体。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Montevideo, Uruguay
- Founded
- 1946
- Website
- urufarma.com.uy
- Categories
- 医疗保健用品, 农业及原材料, 车辆零配件
- Markets
- 乌拉圭, 阿根廷, 智利, 玻利维亚, 秘鲁, 哥伦比亚, 墨西哥
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
- product-authorised-for-sale (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
- debarment-clear (green), checked 2026-08-12 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-12 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- registered-manufacturer (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
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)
- Vehicle parts affecting safety sold in Europe generally require UNECE type approval (E-mark). UNECE