Meridian Medical, razvoj, proizvodnja in prodaja medicinskih pripomočkov, d.o.o.
Fabricante e exportador industrial esloveno
Meridian Medical, razvoj, proizvodnja in prodaja medicinskih pripomočkov, d.o.o. é listada pela Sloexport no outro setor manufatureiro. Seu perfil de diretório descreve operações, incluindo A empresa privada, com mais de 20 anos de experiência no campo de laser oftálmico, é um produtor de nicho de sistemas de laser médico para oftalmologia. O que torna os produtos OPHTHALL especiais é que a tecnologia laser de ponta, que é a nossa paixão e experiência, é cuidadosamente equilibrada entre a manipulação para médicos e.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Ljubljana - Šentvid, Slovenia
- Website
- https://ophthall.com
- Categories
- Fabricação farmacêutica, Suprimentos médicos e de saúde
- Markets
- Eslovênia, Áustria, Alemanha, Itália, Croácia
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)