Zarys International Group Sp. z o.o.
Set di infusione, siringhe e articoli monouso medici polacchi per la vendita all'ingrosso ospedaliera.
Zarys International Group produce set per infusione, apparecchiature per trasfusione di sangue, siringhe, cateteri e guanti da esplorazione a Zabrze, Slesia. Uno dei maggiori produttori polacchi di dispositivi medici monouso, rifornisce ospedali pubblici, grossisti farmaceutici e distributori sanitari in tutta l'Europa centrale e orientale.
- Type
- brand seeking distribution
- Location
- Zabrze, Poland
- Founded
- 1989
- Website
- zarys.com
- Categories
- Forniture medicali e sanitarie
- Markets
- Polonia, Germania, Cechia, Ungheria, Romania
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-10 Mail server of the company domain
- domain-registered (green), checked 2026-08-10 Domain registry record
- registry-activity (green), checked 2026-08-21 REGON national business register (GUS, Poland)
- registered-address (green), checked 2026-08-20 Ministry of Finance VAT white list (Poland)
- registered-since (green), checked 2003-10-01 Ministry of Finance VAT white list (Poland)
- tax-filing-active (green), checked 2026-08-20 Ministry of Finance VAT white list (Poland)
- public-contract-awarded (green), checked 2026-08-20 TED (Tenders Electronic Daily), EU public procurement award notices Qui l'aggiudicazione porta con sé anche un controllo altrui: nell'UE e nello SEE la stazione appaltante deve escludere gli operatori condannati per frode, corruzione o riciclaggio e quelli con debiti fiscali o contributivi accertati con decisione definitiva. Directive 2014/24/EU, Article 57 (exclusion grounds)
- export-registered (green), checked 2026-08-10 EU EORI validation (European Commission)
- debarment-clear (green), checked 2026-08-10 OpenSanctions
- sanctions-clear (green), checked 2026-08-10 OpenSanctions
- vat-valid (green), checked 2026-08-10 VIES
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
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)