Eriplast spa
Eriplast
Starting from the storage of the material in external silos, passing through a new automated transportation system managed by an integrated software, arriving to the extrusion lines, Eriplast guarantees the complete traceability of the production process.
- Type
- Manufacturer
- Location
- Bassano del Grappa, Italy
- Website
- eriplast.it
- Categories
- Medical & Healthcare Supplies, Packaging & Printing Supplies, Industrial Machinery
Listed in a source registry
Verified facts
- state-aid-sector (green), checked 2026-02-02 Registro Nazionale degli Aiuti di Stato (rna.gov.it), open data
- vat-valid (green), checked 2026-08-16 VIES (European Commission)
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)
- Machinery sold in the EU needs CE marking with a declaration of conformity under the EU machinery rules. European Commission
- 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