Comarch SA
A Comarch é uma empresa polonesa de TI e desenvolvimento de software que produz sistemas ERP, telecomunicações…
A Comarch é uma empresa polonesa de TI e desenvolvimento de software que produz sistemas ERP, sistemas de suporte de telecomunicações (BSS/OSS), plataformas de comércio eletrônico, TI de saúde e produtos de segurança cibernética para clientes empresariais e PMEs em todo o mundo. A empresa opera mais de 90 escritórios em todo o mundo e produz seu próprio hardware, Comarch IoT, sensores para cidades inteligentes e software para dispositivos médicos, além de fornecer terceirização de TI e serviços em nuvem.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Kraków, Poland
- Founded
- 1993
- Website
- comarch.com
- Categories
- Eletrônicos de consumo, Material e equipamento de escritório, Suprimentos médicos e de saúde
- Markets
- Polônia, Alemanha, França, Itália, Estados Unidos, Reino Unido, Tchéquia
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)