Altura™ Endograft System With Delivery Catheter Gen 2.0 - EUDAMED Registration 05055715637824

Access comprehensive regulatory information for Altura™ Endograft System With Delivery Catheter Gen 2.0 in the European Union medical device market through Pure Global AI's free database. This Class III device is registered with EU EUDAMED under Primary DI 05055715637824 and manufactured by Lombard Medical Limited in United Kingdom (ex Northern Ireland).

This page provides complete registration details including manufacturer information, authorized representative details, competent authority (DE/CA304 - Marktüberwachung Medizinprodukte Bayern), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.