ISE INTERNAL STANDARD GEN.2. - DIGEMID Registration DMDIV5925E

Access comprehensive regulatory information for ISE INTERNAL STANDARD GEN.2. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV5925E and manufactured by ROCHE DIAGNOSTICS GMBH. The device was registered on December 19, 2024.

This page provides complete registration details including product type (IN VITRO 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.