Meridian Medical, razvoj, proizvodnja in prodaja medicinskih pripomočkov, d.o.o.
Slovenian industrial manufacturer and exporter
Meridian Medical, razvoj, proizvodnja in prodaja medicinskih pripomočkov, d.o.o. is listed by Sloexport in the other manufacturing sector. Its directory profile describes operations including The private owned company, with more than 20 years of experiences in ophthalmic laser field, is a niche producer of ophthalmology medical laser systems. What makes OPHTHALL products special is that high end laser technology, which is our passion and expertise, is carefully balanced between manipulation for doctors and.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Ljubljana - Šentvid, Slovenia
- Website
- https://ophthall.com
- Categories
- Pharmaceutical Manufacturing, Medical & Healthcare Supplies
- Markets
- Slovenia, Austria, Germany, Italy, Croatia
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)