Meridian Medical, razvoj, proizvodnja in prodaja medicinskih pripomočkov, d.o.o.
Fabricant industriel et exportateur slovène
Meridian Medical, cabinet, proizvodnja in prodaja medicinskih pripomočkov, d.o.o. est répertorié par Sloexport dans le secteur des autres industries manufacturières. Son profil d'annuaire décrit les opérations notamment. L'entreprise privée, avec plus de 20 ans d'expérience dans le domaine du laser ophtalmique, est un producteur de niche de systèmes laser médicaux ophtalmologiques. Ce qui rend les produits OPHTHALL spéciaux, c'est que la technologie laser haut de gamme, qui est notre passion et notre expertise, est soigneusement équilibrée entre manipulation pour les médecins et.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Ljubljana - Šentvid, Slovenia
- Website
- https://ophthall.com
- Categories
- Production pharmaceutique, Fournitures médicales et de santé
- Markets
- Slovénie, Autriche, Allemagne, Italie, Croatie
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)