Mediso Medical Imaging Systems Kft.
Produsen pengobatan nuklir dan sistem pencitraan praklinis Hongaria.
Mediso memproduksi SPECT, PET, CT, MRI, dan sistem pencitraan medis multimodal di Hongaria. Didirikan pada tahun 1990, perusahaan ini memasok rumah sakit, lembaga penelitian, dan distributor perangkat medis di seluruh dunia.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Budapest, Hungary
- Founded
- 1990
- Website
- mediso.com
- Categories
- Perlengkapan Medis & Kesehatan, Elektronik Konsumen
- Markets
- Hungaria, Jerman, Amerika Serikat, Jepang
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
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- domain-registered (green), checked 2026-08-09 Domain registry record
- public-contract-awarded (green), checked 2026-08-02 TED, EU public procurement bulletin Di sini kemenangan tender juga membawa pemeriksaan pihak lain: di UE dan EEA, pembeli publik wajib menggugurkan peserta yang dipidana karena penipuan, korupsi, atau pencucian uang, serta yang tunggakan pajak atau iurannya ditetapkan lewat putusan final. Directive 2014/24/EU, Article 57 (exclusion grounds)
- 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)