BIOSTEP LP - EUDAMED Registration 00713980022442

Access comprehensive regulatory information for BIOSTEP LP in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 00713980022442 and manufactured by Alps South, LLC in United States.

This page provides complete registration details including trade name (BioStep LP, Size 25, Right, Rate C, Dark), manufacturer information, authorized representative details, competent authority (Ministerie van Volksgezondheid, Welzijn en Sport), 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.