SteriPack
Conception, fabrication de dispositifs médicaux et produits de conditionnement pharmaceutique.
SteriPack fabrique des produits de conception, de fabrication et d'emballage pharmaceutique de dispositifs médicaux à partir de ses opérations de Mullingar. La société fournit des systèmes de santé, des laboratoires, des partenaires OEM ou des clients exportateurs réglementés sur ses principaux marchés cotés.
- Type
- brand seeking distribution
- Location
- Mullingar, Ireland
- Founded
- 1994
- Website
- steripack.com
- Categories
- Fournitures médicales et de santé, Emballage et fournitures d'impression
- Markets
- Irlande, États-Unis, Royaume-Uni, Allemagne
Verified facts
- debarment-clear (green), checked 2026-08-12 OpenSanctions
- sanctions-clear (green), checked 2026-08-12 OpenSanctions
Claimed certifications
- 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)
- 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)
- No public registry exists for certificates of this kind in this sector: conformity is declared by the manufacturer. European Commission: CE marking, manufacturer's conformity assessment