Meridian Medical, razvoj, proizvodnja in prodaja medicinskih pripomočkov, d.o.o.
スロベニアの工業製造業者および輸出業者
Meridian Medical、ラズボイ、prodaja medicinskih primočkov、d.o.o.のproizvodnja。 Sloexport によりその他の製造部門に上場されています。同社のディレクトリ プロフィールには、次のような事業内容が記載されています。この非公開会社は、眼科用レーザー分野で 20 年以上の経験があり、眼科用医療レーザー システムのニッチなメーカーです。 OPHTHALL 製品を特別なものにしているのは、私たちの情熱と専門知識であるハイエンドのレーザー技術が、医師のための操作と医師のための操作の間で慎重にバランスが取れていることです。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Ljubljana - Šentvid, Slovenia
- Website
- https://ophthall.com
- Categories
- 医薬品製造, 医療およびヘルスケア用品
- Markets
- スロベニア, オーストリア, ドイツ, イタリア, クロアチア
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)