Mediso Medical Imaging Systems Kft.
Macar nükleer tıp ve klinik öncesi görüntüleme sistemi üreticisi.
Mediso, Macaristan'da SPECT, PET, CT, MRI ve multimodal tıbbi görüntüleme sistemleri üretmektedir. 1990 yılında kurulan şirket, dünya çapında hastanelere, araştırma kurumlarına ve tıbbi cihaz distribütörlerine ürün tedarik etmektedir.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Budapest, Hungary
- Founded
- 1990
- Website
- mediso.com
- Categories
- Tıbbi ve Sağlık Malzemeleri, Tüketici Elektroniği
- Markets
- Macaristan, Almanya, Amerika Birleşik Devletleri, Japonya
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 Burada ihalenin kazanılması başkasının yaptığı bir denetimi de taşır: AB ve AEA'da kamu alıcısı, dolandırıcılık, yolsuzluk veya kara para aklamadan hüküm giymiş istekliler ile kesinleşmiş kararla vergi veya sosyal güvenlik borcu saptananları elemek zorundadır. 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)