GUIDE WIRE. - DIGEMID Registration DM24060E

Access comprehensive regulatory information for GUIDE WIRE. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DM24060E and manufactured by ADRIA S.R.L.. The device was registered on July 20, 2022.

This page provides complete registration details including product type (MEDICAL DEVICE), manufacturer information, authorized representative details, and regulatory compliance data from the official Peru DIGEMID medical device database. Pure Global AI offers free access to Peru's complete medical device registry.