Comarch SA
Comarch is een Pools IT- en softwareontwikkelingsbedrijf dat ERP-systemen, telecommunicatie…
Comarch is een Pools IT- en softwareontwikkelingsbedrijf dat ERP-systemen, telecommunicatie-ondersteuningssystemen (BSS/OSS), e-commerceplatforms, IT in de gezondheidszorg en cyberbeveiligingsproducten produceert voor zakelijke en MKB-klanten over de hele wereld. Het bedrijf heeft wereldwijd meer dan 90 kantoren en produceert zijn eigen hardware, Comarch IoT, slimme stadssensoren en software voor medische apparatuur, en levert ook IT-outsourcing en clouddiensten.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Kraków, Poland
- Founded
- 1993
- Website
- comarch.com
- Categories
- Consumentenelektronica, Kantoorbenodigdheden en -apparatuur, Medische en gezondheidszorgbenodigdheden
- Markets
- Polen, Duitsland, Frankrijk, Italië, Verenigde Staten, Verenigd Koninkrijk, Tsjechië
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)