Meridian Medical, razvoj, proizvodnja in prodaja medicinskih pripomočkov, d.o.o.
Produsen dan eksportir industri Slovenia
Meridian Medical, razvoj, proizvodnja di prodaja medicinskih pripomočkov, d.o.o. terdaftar oleh Sloexport di sektor manufaktur lainnya. Profil direktorinya menjelaskan operasi termasuk Perusahaan milik swasta, dengan lebih dari 20 tahun pengalaman di bidang laser mata, adalah produsen khusus sistem laser medis oftalmologi. Apa yang membuat produk OPHTHALL istimewa adalah teknologi laser kelas atas, yang merupakan semangat dan keahlian kami, yang secara cermat diseimbangkan antara manipulasi untuk dokter dan.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Ljubljana - Šentvid, Slovenia
- Website
- https://ophthall.com
- Categories
- Manufaktur Farmasi, Perlengkapan Medis & Kesehatan
- Markets
- Slovenia, Austria, Jerman, Italia, Kroasia
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)