Meridian Medical, razvoj, proizvodnja in prodaja medicinskih pripomočkov, d.o.o.
Fabricante y exportador industrial esloveno
Meridian Medical, razvoj, proizvodnja in prodaja medicinskih pripomočkov, d.o.o. cotiza en Sloexport en el otro sector manufacturero. El perfil de su directorio describe operaciones que incluyen. La empresa de propiedad privada, con más de 20 años de experiencia en el campo del láser oftálmico, es un productor especializado de sistemas láser médicos para oftalmología. Lo que hace que los productos OPHTHALL sean especiales es que la tecnología láser de alta gama, que es nuestra pasión y experiencia, se equilibra cuidadosamente entre manipulación para médicos y.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Ljubljana - Šentvid, Slovenia
- Website
- https://ophthall.com
- Categories
- Fabricación farmacéutica, Suministros médicos y sanitarios
- Markets
- Eslovenia, Austria, Alemania, Italia, Croacia
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)