Comarch SA
Comarch, ERP sistemleri, telekomünikasyon ürünleri üreten Polonyalı bir BT ve yazılım geliştirme şirketidir…
Comarch, dünya çapındaki kurumsal ve KOBİ müşterileri için ERP sistemleri, telekomünikasyon destek sistemleri (BSS/OSS), e-ticaret platformları, sağlık hizmetleri BT ve siber güvenlik ürünleri üreten Polonyalı bir BT ve yazılım geliştirme şirketidir. Şirket dünya çapında 90'dan fazla ofisi işletiyor ve kendi donanımını, Comarch IoT'yi, akıllı şehir sensörlerini ve tıbbi cihaz yazılımını üretmenin yanı sıra BT dış kaynak kullanımı ve bulut hizmetleri de sağlıyor.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Kraków, Poland
- Founded
- 1993
- Website
- comarch.com
- Categories
- Tüketici Elektroniği, Ofis Malzemeleri ve Ekipmanları, Tıbbi ve Sağlık Malzemeleri
- Markets
- Polonya, Almanya, Fransa, İtalya, Amerika Birleşik Devletleri, Birleşik Krallık, Çekya
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 2026-08-08 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- domain-registered (green), checked 2026-08-08 Domain registry record
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- ISO 14001, Environmental Management IAF CertSearch
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)
- If the goods are paper, board or printed products, EU imports fall under the Deforestation Regulation (EUDR) due-diligence regime; packaging machinery itself does not. European Commission (EUDR)