Urufarma S.A.
1946년부터 호르몬 및 종양학 제품을 전문으로 하는 우루과이 제약 제조업체
Urufarma는 몬테비데오에 본사를 둔 제약 제조업체로 50개 이상의 국가에 수출할 호르몬 제품, 경구 피임약, 종양학 의약품을 생산합니다. 회사는 GLP 인증을 보유하고 있으며 최근 카라스코 공항 근처에 새로운 산업 단지를 개장했습니다.
- 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
- 의료 및 건강 관리 용품, 농업 및 원자재, 차량 부품 및 액세서리
- Markets
- 우루과이, 아르헨티나, 칠레, 볼리비아, 페루, 콜롬비아, 멕시코
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