STERIS Laboratories Inc
अनुबंध बंध्याकरण एवं प्रयोगशाला परीक्षण सेवाएँ | स्टेरिस एएसटी
STERIS AST चिकित्सा उपकरण और दवा निर्माताओं को अनुबंध स्टरलाइज़ेशन, प्रयोगशाला परीक्षण और उत्पाद और पैकेजिंग परीक्षण सेवाएँ प्रदान करता है।
- Type
- Manufacturer
- Location
- Malaysia
- Website
- https://steris-labs.com
- Categories
- फार्मास्युटिकल विनिर्माण, चिकित्सा एवं स्वास्थ्य देखभाल आपूर्तियाँ, पैकेजिंग एवं मुद्रण आपूर्तियाँ
Verified facts
- domain-registered (green), checked 2026-08-09 Domain registry record
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- debarment-clear (green), checked 2026-08-09 OpenSanctions
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)
- Paper and printed products imported into the EU fall under the Deforestation Regulation (EUDR) due-diligence regime. European Commission (EUDR)
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)