Meridian Medical, razvoj, proizvodnja in prodaja medicinskih pripomočkov, d.o.o.
슬로베니아 산업 제조업체 및 수출업체
Meridian Medical, razvoj, proizvodnja in prodaja medicinskih pripomočkov, d.o.o. Sloexport에 의해 기타 제조 부문에 상장되어 있습니다. 디렉토리 프로필에는 안과 레이저 분야에서 20년 이상의 경험을 보유한 개인 소유 회사인 안과 의료 레이저 시스템의 틈새 생산업체를 포함한 운영이 설명되어 있습니다. OPHTHALL 제품을 특별하게 만드는 것은 우리의 열정과 전문성인 첨단 레이저 기술이 의사를 위한 시술과 시술 사이에서 신중하게 균형을 이루고 있다는 것입니다.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Ljubljana - Šentvid, Slovenia
- Website
- https://ophthall.com
- Categories
- 의약품 제조, 의료 및 건강 관리 용품
- Markets
- 슬로베니아, 오스트리아, 독일, 이탈리아, 크로아티아
Listed in a source registry
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 2026-08-09 Domain registry record
- sanctions-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
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)
- 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)