Zarys International Group Sp. z o.o.
Polish infusion sets, syringes and medical disposables OEM for hospital wholesale.
Zarys International Group manufactures infusion sets, blood transfusion equipment, syringes, catheters and examination gloves in Zabrze, Silesia. One of the largest Polish producers of medical disposables, it supplies public hospitals, pharmaceutical wholesalers and healthcare distributors across Central and Eastern Europe.
- Type
- Manufacturer
- Location
- Zabrze, Poland
- Founded
- 1989
- Website
- zarys.com
- Categories
- Medical & Healthcare Supplies
- Markets
- Poland, Germany, Czechia, Hungary, 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)
- vat-valid (green), checked 2026-08-10 VIES
- 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 Here the award carries someone else's check: in the EU and the EEA a public buyer must exclude bidders convicted of fraud, corruption or money laundering, and those found by a final decision to owe taxes or social contributions. 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
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)