SteriPack
Diseño de dispositivos médicos, fabricación y envasado de productos farmacéuticos.
SteriPack fabrica productos de diseño, fabricación y embalaje farmacéutico de dispositivos médicos desde sus operaciones de Mullingar. La empresa suministra sistemas de atención médica, laboratorios, socios OEM o clientes de exportación regulados en sus mercados primarios listados.
- Type
- brand seeking distribution
- Location
- Mullingar, Ireland
- Founded
- 1994
- Website
- steripack.com
- Categories
- Suministros médicos y sanitarios, Embalaje y suministros de impresión
- Markets
- Irlanda, Estados Unidos, Reino Unido, Alemania
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