K-MOD REV INSTRUMENTS, K-MOD REV TIBIAL INSTRUMENTS SET, K-MOD REV FEMORAL INSTRUMENTS SET, K-MOD REV REAMERS SET, K-MOD REV COMMON INSTRUMENTS SET, K-MOD REV FEMORAL TRIALS SET, K-MOD REV UC-DC HIGH INSERT TRIALS SET.

Access comprehensive regulatory information for K-MOD REV INSTRUMENTS, K-MOD REV TIBIAL INSTRUMENTS SET, K-MOD REV FEMORAL INSTRUMENTS SET, K-MOD REV REAMERS SET, K-MOD REV COMMON INSTRUMENTS SET, K-MOD REV FEMORAL TRIALS SET, K-MOD REV UC-DC HIGH INSERT TRIALS SET. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DM17604E and manufactured by GRUPPO BIOIMPIANTI S.R.L.. The device was registered on August 27, 2019.

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.