Comarch SA
Comarch adalah perusahaan TI dan pengembangan perangkat lunak Polandia yang memproduksi sistem ERP, telekomunikasi…
Comarch adalah perusahaan TI dan pengembangan perangkat lunak asal Polandia yang memproduksi sistem ERP, sistem pendukung telekomunikasi (BSS/OSS), platform e-niaga, TI layanan kesehatan, dan produk keamanan siber untuk pelanggan perusahaan dan UKM di seluruh dunia. Perusahaan ini mengoperasikan lebih dari 90 kantor di seluruh dunia dan memproduksi perangkat kerasnya sendiri, Comarch IoT, sensor kota pintar, dan perangkat lunak perangkat medis, serta menyediakan outsourcing TI dan layanan cloud.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Kraków, Poland
- Founded
- 1993
- Website
- comarch.com
- Categories
- Elektronik Konsumen, Perlengkapan & Peralatan Kantor, Perlengkapan Medis & Kesehatan
- Markets
- Polandia, Jerman, Prancis, Italia, Amerika Serikat, Inggris Raya, Ceko
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)